{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Recurrent+Wilms+Tumor&page=2",
    "query": {
      "condition": "Recurrent Wilms Tumor",
      "page": 2
    },
    "page_size": 10
  },
  "pagination": {
    "page": 2,
    "page_size": 10,
    "total_count": 10,
    "total_pages": 1,
    "next_page_url": null,
    "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Recurrent+Wilms+Tumor&page=1&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-06-25T13:45:40.603Z",
  "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.",
  "notes": [
    "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.",
    "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.",
    "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees."
  ],
  "trials": [
    {
      "nct_id": "NCT05985161",
      "title": "A Study of Selinexor in People With Wilms Tumors and Other Solid Tumors",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE2"
      ],
      "conditions": [
        "Wilms Tumor",
        "Rhabdoid Tumor",
        "Malignant Peripheral Nerve Sheath Tumors",
        "MPNST",
        "Nephroblastoma",
        "XPO1 Gene Mutation",
        "Solid Tumor"
      ],
      "interventions": [
        {
          "name": "Selinexor",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Memorial Sloan Kettering Cancer Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "12 Months",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "12 Months and older"
      },
      "enrollment_count": 45,
      "start_date": "2023-08-01",
      "completion_date": "2029-08-01",
      "has_results": false,
      "last_update_posted_date": "2026-05-06",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 16,
      "location_summary": "Los Angeles, California • Palo Alto, California • Washington D.C., District of Columbia + 13 more",
      "locations": [
        {
          "city": "Los Angeles",
          "state": "California"
        },
        {
          "city": "Palo Alto",
          "state": "California"
        },
        {
          "city": "Washington D.C.",
          "state": "District of Columbia"
        },
        {
          "city": "Atlanta",
          "state": "Georgia"
        },
        {
          "city": "Chicago",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05985161"
    },
    {
      "nct_id": "NCT02867592",
      "title": "Cabozantinib-S-Malate in Treating Younger Patients With Recurrent, Refractory, or Newly Diagnosed Sarcomas, Wilms Tumor, or Other Rare Tumors",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE2"
      ],
      "conditions": [
        "Adrenal Cortical Carcinoma",
        "Alveolar Soft Part Sarcoma",
        "Central Nervous System Neoplasm",
        "Childhood Clear Cell Sarcoma of Soft Tissue",
        "Clear Cell Sarcoma of Soft Tissue",
        "Ewing Sarcoma",
        "Hepatoblastoma",
        "Hepatocellular Carcinoma",
        "Osteosarcoma",
        "Recurrent Adrenal Cortical Carcinoma",
        "Recurrent Alveolar Soft Part Sarcoma",
        "Recurrent Clear Cell Sarcoma of Soft Tissue",
        "Recurrent Ewing Sarcoma",
        "Recurrent Hepatoblastoma",
        "Recurrent Hepatocellular Carcinoma",
        "Recurrent Kidney Wilms Tumor",
        "Recurrent Malignant Solid Neoplasm",
        "Recurrent Osteosarcoma",
        "Recurrent Primary Malignant Central Nervous System Neoplasm",
        "Recurrent Renal Cell Carcinoma",
        "Recurrent Rhabdomyosarcoma",
        "Recurrent Soft Tissue Sarcoma",
        "Recurrent Thyroid Gland Medullary Carcinoma",
        "Refractory Adrenal Cortical Carcinoma",
        "Refractory Alveolar Soft Part Sarcoma",
        "Refractory Clear Cell Sarcoma of Soft Tissue",
        "Refractory Ewing Sarcoma",
        "Refractory Hepatoblastoma",
        "Refractory Hepatocellular Carcinoma",
        "Refractory Malignant Solid Neoplasm",
        "Refractory Osteosarcoma",
        "Refractory Primary Central Nervous System Neoplasm",
        "Refractory Primary Malignant Central Nervous System Neoplasm",
        "Refractory Renal Cell Carcinoma",
        "Refractory Rhabdomyosarcoma",
        "Refractory Soft Tissue Sarcoma",
        "Refractory Thyroid Gland Medullary Carcinoma",
        "Refractory Wilms Tumor",
        "Renal Cell Carcinoma",
        "Rhabdomyosarcoma",
        "Soft Tissue Sarcoma",
        "Solid Neoplasm",
        "Thyroid Gland Medullary Carcinoma",
        "Wilms Tumor"
      ],
      "interventions": [
        {
          "name": "Cabozantinib",
          "type": "DRUG"
        },
        {
          "name": "Cabozantinib S-malate",
          "type": "DRUG"
        },
        {
          "name": "Pharmacological Study",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "DRUG",
        "OTHER"
      ],
      "sponsor": "National Cancer Institute (NCI)",
      "sponsor_class": "NIH",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "2 Years",
        "maximum_age": "30 Years",
        "sex": "ALL",
        "summary": "2 Years to 30 Years"
      },
      "enrollment_count": 109,
      "start_date": "2017-05-18",
      "completion_date": "2026-06-27",
      "has_results": true,
      "last_update_posted_date": "2026-06-11",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 142,
      "location_summary": "Birmingham, Alabama • Anchorage, Alaska • Little Rock, Arkansas + 104 more",
      "locations": [
        {
          "city": "Birmingham",
          "state": "Alabama"
        },
        {
          "city": "Anchorage",
          "state": "Alaska"
        },
        {
          "city": "Little Rock",
          "state": "Arkansas"
        },
        {
          "city": "Anaheim",
          "state": "California"
        },
        {
          "city": "Bellflower",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02867592"
    },
    {
      "nct_id": "NCT00002673",
      "title": "Immunotherapy in Treating Patients Who Are Undergoing Bone Marrow or Peripheral Stem Cell Transplantation",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE2"
      ],
      "conditions": [
        "Cancer"
      ],
      "interventions": [
        {
          "name": "infection prophylaxis and management",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Fred Hutchinson Cancer Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "12 Years",
        "maximum_age": "60 Years",
        "sex": "ALL",
        "summary": "12 Years to 60 Years"
      },
      "enrollment_count": 30,
      "start_date": "1995-06",
      "completion_date": "2002-02",
      "has_results": false,
      "last_update_posted_date": "2010-06-17",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 1,
      "location_summary": "Seattle, Washington",
      "locations": [
        {
          "city": "Seattle",
          "state": "Washington"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00002673"
    },
    {
      "nct_id": "NCT04195555",
      "title": "Ivosidenib in Treating Patients With Advanced Solid Tumors, Lymphoma, or Histiocytic Disorders With IDH1 Mutations (A Pediatric MATCH Treatment Trial)",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE2"
      ],
      "conditions": [
        "Recurrent Ependymoma",
        "Recurrent Ewing Sarcoma",
        "Recurrent Hepatoblastoma",
        "Recurrent Langerhans Cell Histiocytosis",
        "Recurrent Malignant Germ Cell Tumor",
        "Recurrent Malignant Glioma",
        "Recurrent Malignant Solid Neoplasm",
        "Recurrent Medulloblastoma",
        "Recurrent Neuroblastoma",
        "Recurrent Non-Hodgkin Lymphoma",
        "Recurrent Osteosarcoma",
        "Recurrent Peripheral Primitive Neuroectodermal Tumor",
        "Recurrent Rhabdoid Tumor",
        "Recurrent Rhabdomyosarcoma",
        "Recurrent Soft Tissue Sarcoma",
        "Recurrent WHO Grade 2 Glioma",
        "Refractory Ependymoma",
        "Refractory Ewing Sarcoma",
        "Refractory Hepatoblastoma",
        "Refractory Langerhans Cell Histiocytosis",
        "Refractory Malignant Germ Cell Tumor",
        "Refractory Malignant Glioma",
        "Refractory Malignant Solid Neoplasm",
        "Refractory Medulloblastoma",
        "Refractory Neuroblastoma",
        "Refractory Non-Hodgkin Lymphoma",
        "Refractory Osteosarcoma",
        "Refractory Peripheral Primitive Neuroectodermal Tumor",
        "Refractory Rhabdoid Tumor",
        "Refractory Rhabdomyosarcoma",
        "Refractory Soft Tissue Sarcoma",
        "Refractory WHO Grade 2 Glioma",
        "Wilms Tumor"
      ],
      "interventions": [
        {
          "name": "Ivosidenib",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "National Cancer Institute (NCI)",
      "sponsor_class": "NIH",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "12 Months",
        "maximum_age": "21 Years",
        "sex": "ALL",
        "summary": "12 Months to 21 Years"
      },
      "enrollment_count": 3,
      "start_date": "2020-07-20",
      "completion_date": "2027-05-09",
      "has_results": true,
      "last_update_posted_date": "2026-06-17",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 171,
      "location_summary": "Birmingham, Alabama • Anchorage, Alaska • Mesa, Arizona + 129 more",
      "locations": [
        {
          "city": "Birmingham",
          "state": "Alabama"
        },
        {
          "city": "Anchorage",
          "state": "Alaska"
        },
        {
          "city": "Mesa",
          "state": "Arizona"
        },
        {
          "city": "Phoenix",
          "state": "Arizona"
        },
        {
          "city": "Tucson",
          "state": "Arizona"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04195555"
    },
    {
      "nct_id": "NCT00036959",
      "title": "ABT-751 in Treating Young Patients With Refractory Solid Tumors",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1"
      ],
      "conditions": [
        "Brain and Central Nervous System Tumors",
        "Childhood Germ Cell Tumor",
        "Extragonadal Germ Cell Tumor",
        "Kidney Cancer",
        "Liver Cancer",
        "Neuroblastoma",
        "Ovarian Cancer",
        "Sarcoma",
        "Unspecified Childhood Solid Tumor, Protocol Specific"
      ],
      "interventions": [
        {
          "name": "ABT-751",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "National Institutes of Health Clinical Center (CC)",
      "sponsor_class": "NIH",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": null,
        "maximum_age": "18 Years",
        "sex": "ALL",
        "summary": "Up to 18 Years"
      },
      "enrollment_count": 90,
      "start_date": "2002-03",
      "completion_date": "2010-02",
      "has_results": false,
      "last_update_posted_date": "2012-03-15",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 3,
      "location_summary": "Chicago, Illinois • Bethesda, Maryland • Philadelphia, Pennsylvania",
      "locations": [
        {
          "city": "Chicago",
          "state": "Illinois"
        },
        {
          "city": "Bethesda",
          "state": "Maryland"
        },
        {
          "city": "Philadelphia",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00036959"
    },
    {
      "nct_id": "NCT06917885",
      "title": "CUE-102 in Recurrent Glioblastoma",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1"
      ],
      "conditions": [
        "Recurrent Glioblastoma",
        "Glioblastoma",
        "Glioma, Malignant"
      ],
      "interventions": [
        {
          "name": "CUE-102",
          "type": "BIOLOGICAL"
        }
      ],
      "intervention_types": [
        "BIOLOGICAL"
      ],
      "sponsor": "David Reardon, MD",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 18,
      "start_date": "2025-07-30",
      "completion_date": "2028-01-31",
      "has_results": false,
      "last_update_posted_date": "2026-03-05",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 2,
      "location_summary": "Boston, Massachusetts",
      "locations": [
        {
          "city": "Boston",
          "state": "Massachusetts"
        },
        {
          "city": "Boston",
          "state": "Massachusetts"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06917885"
    },
    {
      "nct_id": "NCT04320888",
      "title": "Selpercatinib for the Treatment of Advanced Solid Tumors, Lymphomas, or Histiocytic Disorders With Activating RET Gene Alterations, a Pediatric MATCH Treatment Trial",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE2"
      ],
      "conditions": [
        "Hematopoietic and Lymphatic System Neoplasm",
        "Recurrent Ependymoma",
        "Recurrent Ewing Sarcoma",
        "Recurrent Hepatoblastoma",
        "Recurrent Histiocytic and Dendritic Cell Neoplasm",
        "Recurrent Langerhans Cell Histiocytosis",
        "Recurrent Lymphoma",
        "Recurrent Malignant Germ Cell Tumor",
        "Recurrent Malignant Glioma",
        "Recurrent Malignant Solid Neoplasm",
        "Recurrent Medulloblastoma",
        "Recurrent Neuroblastoma",
        "Recurrent Non-Hodgkin Lymphoma",
        "Recurrent Osteosarcoma",
        "Recurrent Peripheral Primitive Neuroectodermal Tumor",
        "Recurrent Rhabdoid Tumor",
        "Recurrent Rhabdomyosarcoma",
        "Recurrent Soft Tissue Sarcoma",
        "Recurrent WHO Grade 2 Glioma",
        "Refractory Ependymoma",
        "Refractory Ewing Sarcoma",
        "Refractory Hepatoblastoma",
        "Refractory Histiocytic and Dendritic Cell Neoplasm",
        "Refractory Langerhans Cell Histiocytosis",
        "Refractory Lymphoma",
        "Refractory Malignant Germ Cell Tumor",
        "Refractory Malignant Glioma",
        "Refractory Malignant Solid Neoplasm",
        "Refractory Medulloblastoma",
        "Refractory Neuroblastoma",
        "Refractory Non-Hodgkin Lymphoma",
        "Refractory Osteosarcoma",
        "Refractory Peripheral Primitive Neuroectodermal Tumor",
        "Refractory Rhabdoid Tumor",
        "Refractory Rhabdomyosarcoma",
        "Refractory Soft Tissue Sarcoma",
        "Refractory WHO Grade 2 Glioma",
        "Wilms Tumor"
      ],
      "interventions": [
        {
          "name": "Computed Tomography",
          "type": "PROCEDURE"
        },
        {
          "name": "Magnetic Resonance Imaging",
          "type": "PROCEDURE"
        },
        {
          "name": "Positron Emission Tomography",
          "type": "PROCEDURE"
        },
        {
          "name": "Radionuclide Imaging",
          "type": "PROCEDURE"
        },
        {
          "name": "Selpercatinib",
          "type": "DRUG"
        },
        {
          "name": "X-Ray Imaging",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE",
        "DRUG"
      ],
      "sponsor": "National Cancer Institute (NCI)",
      "sponsor_class": "NIH",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "12 Months",
        "maximum_age": "21 Years",
        "sex": "ALL",
        "summary": "12 Months to 21 Years"
      },
      "enrollment_count": 1,
      "start_date": "2021-05-03",
      "completion_date": "2026-06-30",
      "has_results": true,
      "last_update_posted_date": "2026-06-17",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 172,
      "location_summary": "Birmingham, Alabama • Anchorage, Alaska • Mesa, Arizona + 129 more",
      "locations": [
        {
          "city": "Birmingham",
          "state": "Alabama"
        },
        {
          "city": "Anchorage",
          "state": "Alaska"
        },
        {
          "city": "Mesa",
          "state": "Arizona"
        },
        {
          "city": "Phoenix",
          "state": "Arizona"
        },
        {
          "city": "Tucson",
          "state": "Arizona"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04320888"
    },
    {
      "nct_id": "NCT00003883",
      "title": "Itraconazole Compared With Fluconazole to Prevent Infections in Patients Undergoing Peripheral Stem Cell or Bone Marrow Transplantation",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE3"
      ],
      "conditions": [
        "Cancer"
      ],
      "interventions": [
        {
          "name": "fluconazole",
          "type": "DRUG"
        },
        {
          "name": "itraconazole",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Fred Hutchinson Cancer Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "13 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "13 Years and older"
      },
      "enrollment_count": 578,
      "start_date": "1998-10",
      "completion_date": "2002-07",
      "has_results": false,
      "last_update_posted_date": "2010-04-02",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 2,
      "location_summary": "Seattle, Washington",
      "locations": [
        {
          "city": "Seattle",
          "state": "Washington"
        },
        {
          "city": "Seattle",
          "state": "Washington"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00003883"
    },
    {
      "nct_id": "NCT00101270",
      "title": "Oxaliplatin and Irinotecan in Treating Young Patients With Refractory Solid Tumors or Lymphomas",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1"
      ],
      "conditions": [
        "Childhood Burkitt Lymphoma",
        "Childhood Central Nervous System Germ Cell Tumor",
        "Childhood Diffuse Large Cell Lymphoma",
        "Childhood Grade III Lymphomatoid Granulomatosis",
        "Childhood Immunoblastic Large Cell Lymphoma",
        "Recurrent Childhood Brain Stem Glioma",
        "Recurrent Childhood Cerebellar Astrocytoma",
        "Recurrent Childhood Cerebral Astrocytoma",
        "Recurrent Childhood Ependymoma",
        "Recurrent Childhood Grade III Lymphomatoid Granulomatosis",
        "Recurrent Childhood Large Cell Lymphoma",
        "Recurrent Childhood Liver Cancer",
        "Recurrent Childhood Lymphoblastic Lymphoma",
        "Recurrent Childhood Malignant Germ Cell Tumor",
        "Recurrent Childhood Medulloblastoma",
        "Recurrent Childhood Rhabdomyosarcoma",
        "Recurrent Childhood Small Noncleaved Cell Lymphoma",
        "Recurrent Childhood Soft Tissue Sarcoma",
        "Recurrent Childhood Supratentorial Primitive Neuroectodermal Tumor",
        "Recurrent Childhood Visual Pathway Glioma",
        "Recurrent Colon Cancer",
        "Recurrent Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor",
        "Recurrent Melanoma",
        "Recurrent Nasopharyngeal Cancer",
        "Recurrent Neuroblastoma",
        "Recurrent Osteosarcoma",
        "Recurrent Wilms Tumor and Other Childhood Kidney Tumors",
        "Recurrent/Refractory Childhood Hodgkin Lymphoma",
        "Unspecified Childhood Solid Tumor, Protocol Specific"
      ],
      "interventions": [
        {
          "name": "irinotecan hydrochloride",
          "type": "DRUG"
        },
        {
          "name": "oxaliplatin",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "National Cancer Institute (NCI)",
      "sponsor_class": "NIH",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "1 Year",
        "maximum_age": "21 Years",
        "sex": "ALL",
        "summary": "1 Year to 21 Years"
      },
      "enrollment_count": 24,
      "start_date": "2005-03",
      "completion_date": null,
      "has_results": false,
      "last_update_posted_date": "2013-06-05",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 1,
      "location_summary": "Arcadia, California",
      "locations": [
        {
          "city": "Arcadia",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00101270"
    },
    {
      "nct_id": "NCT01793168",
      "title": "Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford",
      "overall_status": "RECRUITING",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Rare Disorders",
        "Undiagnosed Disorders",
        "Disorders of Unknown Prevalence",
        "Cornelia De Lange Syndrome",
        "Prenatal Benign Hypophosphatasia",
        "Perinatal Lethal Hypophosphatasia",
        "Odontohypophosphatasia",
        "Adult Hypophosphatasia",
        "Childhood-onset Hypophosphatasia",
        "Infantile Hypophosphatasia",
        "Hypophosphatasia",
        "Kabuki Syndrome",
        "Bohring-Opitz Syndrome",
        "Narcolepsy Without Cataplexy",
        "Narcolepsy-cataplexy",
        "Hypersomnolence Disorder",
        "Idiopathic Hypersomnia Without Long Sleep Time",
        "Idiopathic Hypersomnia With Long Sleep Time",
        "Idiopathic Hypersomnia",
        "Kleine-Levin Syndrome",
        "Kawasaki Disease",
        "Leiomyosarcoma",
        "Leiomyosarcoma of the Corpus Uteri",
        "Leiomyosarcoma of the Cervix Uteri",
        "Leiomyosarcoma of Small Intestine",
        "Acquired Myasthenia Gravis",
        "Addison Disease",
        "Hyperacusis (Hyperacousis)",
        "Juvenile Myasthenia Gravis",
        "Transient Neonatal Myasthenia Gravis",
        "Williams Syndrome",
        "Lyme Disease",
        "Myasthenia Gravis",
        "Marinesco Sjogren Syndrome(Marinesco-Sjogren Syndrome)",
        "Isolated Klippel-Feil Syndrome",
        "Frasier Syndrome",
        "Denys-Drash Syndrome",
        "Beckwith-Wiedemann Syndrome",
        "Emanuel Syndrome",
        "Isolated Aniridia",
        "Axenfeld-Rieger Syndrome",
        "Aniridia-intellectual Disability Syndrome",
        "Aniridia - Renal Agenesis - Psychomotor Retardation",
        "Aniridia - Ptosis - Intellectual Disability - Familial Obesity",
        "Aniridia - Cerebellar Ataxia - Intellectual Disability",
        "Aniridia - Absent Patella",
        "Aniridia",
        "Peters Anomaly - Cataract",
        "Peters Anomaly",
        "Potocki-Shaffer Syndrome",
        "Silver-Russell Syndrome Due to Maternal Uniparental Disomy of Chromosome 11",
        "Silver-Russell Syndrome Due to Imprinting Defect of 11p15",
        "Silver-Russell Syndrome Due to 11p15 Microduplication",
        "Syndromic Aniridia",
        "WAGR Syndrome",
        "Wolf-Hirschhorn Syndrome",
        "4p16.3 Microduplication Syndrome",
        "4p Deletion Syndrome, Non-Wolf-Hirschhorn Syndrome",
        "Autosomal Recessive Stickler Syndrome",
        "Stickler Syndrome Type 2",
        "Stickler Syndrome Type 1",
        "Stickler Syndrome",
        "Mucolipidosis Type 4",
        "X-linked Spinocerebellar Ataxia Type 4",
        "X-linked Spinocerebellar Ataxia Type 3",
        "X-linked Intellectual Disability - Ataxia - Apraxia",
        "X-linked Progressive Cerebellar Ataxia",
        "X-linked Non Progressive Cerebellar Ataxia",
        "X-linked Cerebellar Ataxia",
        "Vitamin B12 Deficiency Ataxia",
        "Toxic Exposure Ataxia",
        "Unclassified Autosomal Dominant Spinocerebellar Ataxia",
        "Thyroid Antibody Ataxia",
        "Sporadic Adult-onset Ataxia of Unknown Etiology",
        "Spinocerebellar Ataxia With Oculomotor Anomaly",
        "Spinocerebellar Ataxia With Epilepsy",
        "Spinocerebellar Ataxia With Axonal Neuropathy Type 2",
        "Spinocerebellar Ataxia Type 8",
        "Spinocerebellar Ataxia Type 7",
        "Spinocerebellar Ataxia Type 6",
        "Spinocerebellar Ataxia Type 5",
        "Spinocerebellar Ataxia Type 4",
        "Spinocerebellar Ataxia Type 37",
        "Spinocerebellar Ataxia Type 36",
        "Spinocerebellar Ataxia Type 35",
        "Spinocerebellar Ataxia Type 34",
        "Spinocerebellar Ataxia Type 32",
        "Spinocerebellar Ataxia Type 31",
        "Spinocerebellar Ataxia Type 30",
        "Spinocerebellar Ataxia Type 3",
        "Spinocerebellar Ataxia Type 29",
        "Spinocerebellar Ataxia Type 28",
        "Spinocerebellar Ataxia Type 27",
        "Spinocerebellar Ataxia Type 26",
        "Spinocerebellar Ataxia Type 25",
        "Spinocerebellar Ataxia Type 23",
        "Spinocerebellar Ataxia Type 22",
        "Spinocerebellar Ataxia Type 21",
        "Spinocerebellar Ataxia Type 20",
        "Spinocerebellar Ataxia Type 2",
        "Spinocerebellar Ataxia Type 19/22",
        "Spinocerebellar Ataxia Type 18",
        "Spinocerebellar Ataxia Type 17",
        "Spinocerebellar Ataxia Type 16",
        "Spinocerebellar Ataxia Type 15/16",
        "Spinocerebellar Ataxia Type 14",
        "Spinocerebellar Ataxia Type 13",
        "Spinocerebellar Ataxia Type 12",
        "Spinocerebellar Ataxia Type 11",
        "Spinocerebellar Ataxia Type 10",
        "Spinocerebellar Ataxia Type 1 With Axonal Neuropathy",
        "Spinocerebellar Ataxia Type 1",
        "Spinocerebellar Ataxia - Unknown",
        "Spinocerebellar Ataxia - Dysmorphism",
        "Non Progressive Epilepsy and/or Ataxia With Myoclonus as a Major Feature",
        "Spasticity-ataxia-gait Anomalies Syndrome",
        "Spastic Ataxia With Congenital Miosis",
        "Spastic Ataxia - Corneal Dystrophy",
        "Spastic Ataxia",
        "Rare Hereditary Ataxia",
        "Rare Ataxia",
        "Recessive Mitochondrial Ataxia Syndrome",
        "Progressive Epilepsy and/or Ataxia With Myoclonus as a Major Feature",
        "Posterior Column Ataxia - Retinitis Pigmentosa",
        "Post-Stroke Ataxia",
        "Post-Head Injury Ataxia",
        "Post Vaccination Ataxia",
        "Polyneuropathy - Hearing Loss - Ataxia - Retinitis Pigmentosa - Cataract",
        "Muscular Atrophy - Ataxia - Retinitis Pigmentosa - Diabetes Mellitus",
        "Non-hereditary Degenerative Ataxia",
        "Paroxysmal Dystonic Choreathetosis With Episodic Ataxia and Spasticity",
        "Olivopontocerebellar Atrophy - Deafness",
        "NARP Syndrome",
        "Myoclonus - Cerebellar Ataxia - Deafness",
        "Multiple System Atrophy, Parkinsonian Type",
        "Multiple System Atrophy, Cerebellar Type",
        "Multiple System Atrophy",
        "Maternally-inherited Leigh Syndrome",
        "Machado-Joseph Disease Type 3",
        "Machado-Joseph Disease Type 2",
        "Machado-Joseph Disease Type 1",
        "Leigh Syndrome",
        "Late-onset Ataxia With Dementia",
        "Infection or Post Infection Ataxia",
        "GAD Ataxia",
        "Hereditary Episodic Ataxia",
        "Gliadin/Gluten Ataxia",
        "Friedreich Ataxia",
        "Fragile X-associated Tremor/Ataxia Syndrome",
        "Familial Paroxysmal Ataxia",
        "Exposure to Medications Ataxia",
        "Episodic Ataxia With Slurred Speech",
        "Episodic Ataxia Unknown Type",
        "Episodic Ataxia Type 7",
        "Episodic Ataxia Type 6",
        "Episodic Ataxia Type 5",
        "Episodic Ataxia Type 4",
        "Episodic Ataxia Type 3",
        "Episodic Ataxia Type 1",
        "Epilepsy and/or Ataxia With Myoclonus as Major Feature",
        "Early-onset Spastic Ataxia-neuropathy Syndrome",
        "Early-onset Progressive Neurodegeneration - Blindness - Ataxia - Spasticity",
        "Early-onset Cerebellar Ataxia With Retained Tendon Reflexes",
        "Early-onset Ataxia With Dementia",
        "Childhood-onset Autosomal Recessive Slowly Progressive Spinocerebellar Ataxia",
        "Dilated Cardiomyopathy With Ataxia",
        "Cataract - Ataxia - Deafness",
        "Cerebellar Ataxia, Cayman Type",
        "Cerebellar Ataxia With Peripheral Neuropathy",
        "Cerebellar Ataxia - Hypogonadism",
        "Cerebellar Ataxia - Ectodermal Dysplasia",
        "Cerebellar Ataxia - Areflexia - Pes Cavus - Optic Atrophy - Sensorineural Hearing Loss",
        "Brain Tumor Ataxia",
        "Brachydactyly - Nystagmus - Cerebellar Ataxia",
        "Benign Paroxysmal Tonic Upgaze of Childhood With Ataxia",
        "Autosomal Recessive Syndromic Cerebellar Ataxia",
        "Autosomal Recessive Spastic Ataxia With Leukoencephalopathy",
        "Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay",
        "Autosomal Recessive Spastic Ataxia - Optic Atrophy - Dysarthria",
        "Autosomal Recessive Spastic Ataxia",
        "Autosomal Recessive Metabolic Cerebellar Ataxia",
        "Autosomal Dominant Spinocerebellar Ataxia Due to Repeat Expansions That do Not Encode Polyglutamine",
        "Autosomal Recessive Ataxia, Beauce Type",
        "Autosomal Recessive Ataxia Due to Ubiquinone Deficiency",
        "Autosomal Recessive Ataxia Due to PEX10 Deficiency",
        "Autosomal Recessive Degenerative and Progressive Cerebellar Ataxia",
        "Autosomal Recessive Congenital Cerebellar Ataxia Due to MGLUR1 Deficiency",
        "Autosomal Recessive Congenital Cerebellar Ataxia Due to GRID2 Deficiency",
        "Autosomal Recessive Congenital Cerebellar Ataxia",
        "Autosomal Recessive Cerebellar Ataxia-pyramidal Signs-nystagmus-oculomotor Apraxia Syndrome",
        "Autosomal Recessive Cerebellar Ataxia-epilepsy-intellectual Disability Syndrome Due to WWOX Deficiency",
        "Autosomal Recessive Cerebellar Ataxia-epilepsy-intellectual Disability Syndrome Due to TUD Deficiency",
        "Autosomal Recessive Cerebellar Ataxia-epilepsy-intellectual Disability Syndrome Due to KIAA0226 Deficiency",
        "Autosomal Recessive Cerebellar Ataxia-epilepsy-intellectual Disability Syndrome",
        "Autosomal Recessive Cerebellar Ataxia With Late-onset Spasticity",
        "Autosomal Recessive Cerebellar Ataxia Due to STUB1 Deficiency",
        "Autosomal Recessive Cerebellar Ataxia Due to a DNA Repair Defect",
        "Autosomal Recessive Cerebellar Ataxia - Saccadic Intrusion",
        "Autosomal Recessive Cerebellar Ataxia - Psychomotor Retardation",
        "Autosomal Recessive Cerebellar Ataxia - Blindness - Deafness",
        "Autosomal Recessive Cerebellar Ataxia",
        "Autosomal Dominant Spinocerebellar Ataxia Due to a Polyglutamine Anomaly",
        "Autosomal Dominant Spinocerebellar Ataxia Due to a Point Mutation",
        "Autosomal Dominant Spinocerebellar Ataxia Due to a Channelopathy",
        "Autosomal Dominant Spastic Ataxia Type 1",
        "Autosomal Dominant Spastic Ataxia",
        "Autosomal Dominant Optic Atrophy",
        "Ataxia-telangiectasia Variant",
        "Ataxia-telangiectasia",
        "Autosomal Dominant Cerebellar Ataxia, Deafness and Narcolepsy",
        "Autosomal Dominant Cerebellar Ataxia Type 4",
        "Autosomal Dominant Cerebellar Ataxia Type 3",
        "Autosomal Dominant Cerebellar Ataxia Type 2",
        "Autosomal Dominant Cerebellar Ataxia Type 1",
        "Autosomal Dominant Cerebellar Ataxia",
        "Ataxia-telangiectasia-like Disorder",
        "Ataxia With Vitamin E Deficiency",
        "Ataxia With Dementia",
        "Ataxia - Oculomotor Apraxia Type 1",
        "Ataxia - Other",
        "Ataxia - Genetic Diagnosis - Unknown",
        "Acquired Ataxia",
        "Adult-onset Autosomal Recessive Cerebellar Ataxia",
        "Alcohol Related Ataxia",
        "Multiple Endocrine Neoplasia",
        "Multiple Endocrine Neoplasia Type II",
        "Multiple Endocrine Neoplasia Type 1",
        "Multiple Endocrine Neoplasia Type 2",
        "Multiple Endocrine Neoplasia, Type IV",
        "Multiple Endocrine Neoplasia, Type 3",
        "Multiple Endocrine Neoplasia (MEN) Syndrome",
        "Multiple Endocrine Neoplasia Type 2B",
        "Multiple Endocrine Neoplasia Type 2A",
        "Atypical Hemolytic Uremic Syndrome",
        "Atypical HUS",
        "Wiedemann-Steiner Syndrome",
        "Breast Implant-Associated Anaplastic Large Cell Lymphoma",
        "Autoimmune/Inflammatory Syndrome Induced by Adjuvants (ASIA)",
        "Hemophagocytic Lymphohistiocytosis",
        "Behcet&#39;s Disease",
        "Alagille Syndrome",
        "Inclusion Body Myopathy With Early-onset Paget Disease and Frontotemporal Dementia (IBMPFD)",
        "Lowe Syndrome",
        "Pitt Hopkins Syndrome",
        "1p36 Deletion Syndrome",
        "Jansen Type Metaphyseal Chondrodysplasia",
        "Cockayne Syndrome",
        "Chronic Recurrent Multifocal Osteomyelitis",
        "CRMO",
        "Malan Syndrome",
        "Hereditary Sensory and Autonomic Neuropathy Type Ie",
        "VCP Disease",
        "Hypnic Jerking",
        "Sleep Myoclonus",
        "Mollaret Meningitis",
        "Recurrent Viral Meningitis",
        "CRB1",
        "Leber Congenital Amaurosis",
        "Retinitis Pigmentosa",
        "Rare Retinal Disorder",
        "KCNMA1-Channelopathy",
        "Primary Biliary Cirrhosis",
        "ZMYND11",
        "Transient Global Amnesia",
        "Glycogen Storage Disease",
        "Alstrom Syndrome",
        "White Sutton Syndrome",
        "DNM1",
        "EIEE31",
        "Myhre Syndrome",
        "Recurrent Respiratory Papillomatosis",
        "Laryngeal Papillomatosis",
        "Tracheal Papillomatosis",
        "Refsum Disease",
        "Nicolaides Baraitser Syndrome",
        "Leukodystrophy",
        "Tango2",
        "Cauda Equina Syndrome",
        "Rare Gastrointestinal Disorders",
        "Achalasia-Addisonian Syndrome",
        "Achalasia Cardia",
        "Achalasia Icrocephaly Syndrome",
        "Anal Fistula",
        "Congenital Sucrase-Isomaltase Deficiency",
        "Eosinophilic Gastroenteritis",
        "Idiopathic Gastroparesis",
        "Hirschsprung Disease",
        "Rare Inflammatory Bowel Disease",
        "Intestinal Pseudo-Obstruction",
        "Scleroderma",
        "Short Bowel Syndrome",
        "Sacral Agenesis",
        "Sacral Agenesis Syndrome",
        "Caudal Regression",
        "Scheuermann Disease",
        "SMC1A Truncated Mutations (Causing Loss of Gene Function)",
        "Cystinosis",
        "Juvenile Nephropathic Cystinosis",
        "Nephropathic Cystinosis",
        "Kennedy Disease",
        "Spinal Bulbar Muscular Atrophy",
        "Warburg Micro Syndrome",
        "Mucolipidoses",
        "Mitochondrial Diseases",
        "Mitochondrial Aminoacyl-tRNA Synthetases",
        "Mt-aaRS Disorders",
        "Hypertrophic Olivary Degeneration",
        "Non-Ketotic Hyperglycinemia",
        "Fish Odor Syndrome",
        "Halitosis",
        "Isolated Congenital Asplenia",
        "Lambert Eaton (LEMS)",
        "Biliary Atresia",
        "STAG1 Gene Mutation",
        "Coffin Lowry Syndrome",
        "Borjeson-Forssman-Lehman Syndrome",
        "Blau Syndrome",
        "Arginase 1 Deficiency",
        "HSPB8 Myopathy",
        "Beta-Mannosidosis",
        "TBX4 Syndrome",
        "DHDDS Gene Mutations",
        "MAND-MBD5-Associated Neurodevelopmental Disorder",
        "Constitutional Mismatch Repair Deficiency (CMMRD)",
        "SPATA5 Disorder",
        "SPATA5L1 Related Disorder",
        "Acrodysostosis",
        "Multi-systematic Smooth Muscle Dysfunction Syndrome",
        "CRELD1 (Cysteine Rich With EGF Like Domains 1)",
        "GNB1 Syndrome",
        "Pyruvate Dehydrogenase Complex Deficiency Disease",
        "Beta Mannosidosis",
        "Kbg Syndrome",
        "Labrune Syndrome",
        "Metachromatic Leukodystrophy (MLD)",
        "Moyamoya Disease",
        "OPHN1 Syndrome",
        "Oculopharyngeal Muscular Dystrophy (OPMD)",
        "TUBB3 Mutation",
        "WOREE (WWOX-related Epileptic Encephalopathy",
        "SCAR12",
        "Skraban-Deardorff Syndrome",
        "Hereditary Myopathy With Early Respiratory Failure"
      ],
      "interventions": [],
      "intervention_types": [],
      "sponsor": "Sanford Health",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": null,
        "maximum_age": null,
        "sex": "ALL",
        "summary": "Not listed"
      },
      "enrollment_count": 20000,
      "start_date": "2010-07",
      "completion_date": "2100-12",
      "has_results": false,
      "last_update_posted_date": "2025-05-29",
      "last_synced_at": "2026-06-25T13:45:40.603Z",
      "location_count": 1,
      "location_summary": "Sioux Falls, South Dakota",
      "locations": [
        {
          "city": "Sioux Falls",
          "state": "South Dakota"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01793168"
    }
  ]
}