{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Sacroiliac+Disorder&page=2",
    "query": {
      "condition": "Sacroiliac Disorder",
      "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=Sacroiliac+Disorder&page=1&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-07-23T08:23:52.446Z",
  "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": "NCT05712850",
      "title": "Clinical Outcome and Fusion Results Using the SiJoin® Transfixing Sacroiliac Fusion Device",
      "overall_status": "UNKNOWN",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Sacroiliitis",
        "Sacroiliac Joint Dysfunction",
        "Iatrogenic Injury",
        "Osteitis Condensans Ilii",
        "Pelvic Fracture"
      ],
      "interventions": [
        {
          "name": "SiJoin® Transfixing Sacroiliac Fusion Device",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "VG Innovations, LLC",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "85 Years",
        "sex": "ALL",
        "summary": "18 Years to 85 Years"
      },
      "enrollment_count": 25,
      "start_date": "2023-01-19",
      "completion_date": "2025-03-31",
      "has_results": false,
      "last_update_posted_date": "2023-07-24",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "Naples, Florida",
      "locations": [
        {
          "city": "Naples",
          "state": "Florida"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05712850"
    },
    {
      "nct_id": "NCT05870488",
      "title": "iFuse TORQ for the Treatment of Sacroiliac Joint Dysfunction",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Sacroiliac Joint Dysfunction",
        "Sacroiliac; Fusion",
        "Sacroiliac Disorder",
        "Sacroiliac Joint Pain"
      ],
      "interventions": [
        {
          "name": "Use of iFuse TORQ",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "SI-BONE, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "21 Years and older"
      },
      "enrollment_count": 110,
      "start_date": "2023-05-23",
      "completion_date": "2027-11",
      "has_results": false,
      "last_update_posted_date": "2026-02-10",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 14,
      "location_summary": "Napa, California • Santa Monica, California • Shelbyville, Indiana + 11 more",
      "locations": [
        {
          "city": "Napa",
          "state": "California"
        },
        {
          "city": "Santa Monica",
          "state": "California"
        },
        {
          "city": "Shelbyville",
          "state": "Indiana"
        },
        {
          "city": "Leawood",
          "state": "Kansas"
        },
        {
          "city": "Overland Park",
          "state": "Kansas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05870488"
    },
    {
      "nct_id": "NCT05426356",
      "title": "Sacral Fracture Fusion/Fixation for Rapid Rehabilitation",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Fracture;Pelvis",
        "Sacral Fracture",
        "Sacroiliac; Fusion",
        "Fragility Fracture",
        "Insufficiency Fractures",
        "Osteoporosis"
      ],
      "interventions": [
        {
          "name": "Surgical Intervention",
          "type": "DEVICE"
        },
        {
          "name": "Non-Surgical Management",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "OTHER"
      ],
      "sponsor": "SI-BONE, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "60 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "60 Years and older"
      },
      "enrollment_count": 28,
      "start_date": "2022-09-18",
      "completion_date": "2024-06-15",
      "has_results": false,
      "last_update_posted_date": "2024-10-24",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 7,
      "location_summary": "Chicago, Illinois • Lincoln, Nebraska • Livingston, New Jersey + 4 more",
      "locations": [
        {
          "city": "Chicago",
          "state": "Illinois"
        },
        {
          "city": "Lincoln",
          "state": "Nebraska"
        },
        {
          "city": "Livingston",
          "state": "New Jersey"
        },
        {
          "city": "Wyomissing",
          "state": "Pennsylvania"
        },
        {
          "city": "Charleston",
          "state": "South Carolina"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05426356"
    },
    {
      "nct_id": "NCT05279937",
      "title": "The Ultrasound-Guided Dextrose Prolotherapy in Ehlers-Danlos Syndrome Patients",
      "overall_status": "NOT_YET_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE3"
      ],
      "conditions": [
        "Ehlers-Danlos Syndrome",
        "Low Back Pain",
        "Sacroiliac Instability"
      ],
      "interventions": [
        {
          "name": "Dextrose 50% Intravenous Solution",
          "type": "DRUG"
        },
        {
          "name": "Lidocaine 1% Injectable Solution",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Tulane University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "75 Years",
        "sex": "ALL",
        "summary": "18 Years to 75 Years"
      },
      "enrollment_count": 40,
      "start_date": "2026-06",
      "completion_date": "2027-06",
      "has_results": false,
      "last_update_posted_date": "2026-03-02",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "New Orleans, Louisiana",
      "locations": [
        {
          "city": "New Orleans",
          "state": "Louisiana"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05279937"
    },
    {
      "nct_id": "NCT01861899",
      "title": "Treatment of Sacroiliac Dysfunction With SI-LOK® Sacroiliac Joint Fixation SI-SI-LOK",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Joint Dysfunction"
      ],
      "interventions": [
        {
          "name": "SI-LOK",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Globus Medical Inc",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": "70 Years",
        "sex": "ALL",
        "summary": "21 Years to 70 Years"
      },
      "enrollment_count": 46,
      "start_date": "2013-05-02",
      "completion_date": "2019-04-11",
      "has_results": false,
      "last_update_posted_date": "2020-09-11",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "Saint Albans, Vermont",
      "locations": [
        {
          "city": "Saint Albans",
          "state": "Vermont"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01861899"
    },
    {
      "nct_id": "NCT03421535",
      "title": "Opposite SI Joint Stretching for GIRD",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Shoulder Impingement"
      ],
      "interventions": [
        {
          "name": "Sleeper Stretch",
          "type": "PROCEDURE"
        },
        {
          "name": "Opposite SI joint Stretch",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Romano Orthopaedic Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "23 Years",
        "maximum_age": "25 Years",
        "sex": "MALE",
        "summary": "23 Years to 25 Years · Male only"
      },
      "enrollment_count": 23,
      "start_date": "2017-05-23",
      "completion_date": "2017-05-23",
      "has_results": false,
      "last_update_posted_date": "2018-02-05",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "Oak Park, Illinois",
      "locations": [
        {
          "city": "Oak Park",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03421535"
    },
    {
      "nct_id": "NCT00523822",
      "title": "Sacroiliac Orthopedic Blocking and Cervical Spine Function",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Musculoskeletal Diseases"
      ],
      "interventions": [
        {
          "name": "Spinal Manipulative Therapy",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "Logan College of Chiropractic",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "20 Years",
        "maximum_age": "30 Years",
        "sex": "ALL",
        "summary": "20 Years to 30 Years"
      },
      "enrollment_count": null,
      "start_date": null,
      "completion_date": null,
      "has_results": false,
      "last_update_posted_date": "2008-08-05",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "Chesterfield, Missouri",
      "locations": [
        {
          "city": "Chesterfield",
          "state": "Missouri"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00523822"
    },
    {
      "nct_id": "NCT01311479",
      "title": "Osteopathic Manipulation for Female Interstitial Cystitis Patients With Sacroiliac Joint Dysfunction",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Interstitial Cystitis",
        "Sacroiliac Joint Somatic Dysfunction"
      ],
      "interventions": [
        {
          "name": "Osteopathic Manipulation Therapy",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Pelvic and Sexual Health Institute",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "FEMALE",
        "summary": "18 Years and older · Female only"
      },
      "enrollment_count": 40,
      "start_date": "2009-11",
      "completion_date": "2018-10",
      "has_results": false,
      "last_update_posted_date": "2014-04-14",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "Philadelphia, Pennsylvania",
      "locations": [
        {
          "city": "Philadelphia",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01311479"
    },
    {
      "nct_id": "NCT02420041",
      "title": "Comparing the Effects of Ultrasound Versus Fluoroscopy for Sacroiliac Joint Injections",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Sacroiliitis"
      ],
      "interventions": [
        {
          "name": "Active comparator: Fluoroscopic Guided SIJ injection",
          "type": "PROCEDURE"
        },
        {
          "name": "Ultrasound Guided Sacroiliac Joint Injection",
          "type": "PROCEDURE"
        },
        {
          "name": "Havel's Inc. EchoStim (facet tip) 21 Gauge 4\" needle",
          "type": "DEVICE"
        },
        {
          "name": "SonoSite S-nerve",
          "type": "DEVICE"
        },
        {
          "name": "iohexol",
          "type": "DEVICE"
        },
        {
          "name": "triamcinolone/lidocaine",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "PROCEDURE",
        "DEVICE",
        "DRUG"
      ],
      "sponsor": "United States Naval Medical Center, San Diego",
      "sponsor_class": "FED",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 28,
      "start_date": "2012-10",
      "completion_date": "2014-03",
      "has_results": true,
      "last_update_posted_date": "2015-11-13",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "San Diego, California",
      "locations": [
        {
          "city": "San Diego",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02420041"
    },
    {
      "nct_id": "NCT03122119",
      "title": "Effectiveness of Ultrasound Guided Platelet Rich Plasma Injections in the Sacroiliac Joint",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Chronic Low Back Pain",
        "Sacroiliitis",
        "Sacroiliac; Backache",
        "Platelet Rich Plasma",
        "Platelet",
        "Injection Site",
        "Ultrasound Therapy; Complications",
        "Treatment"
      ],
      "interventions": [
        {
          "name": "Platelet Rich Plasma Joint Injection",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Star Spine and Sport",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "80 Years",
        "sex": "ALL",
        "summary": "18 Years to 80 Years"
      },
      "enrollment_count": 51,
      "start_date": "2017-05-01",
      "completion_date": "2022-09-01",
      "has_results": true,
      "last_update_posted_date": "2023-04-28",
      "last_synced_at": "2026-07-23T08:23:52.446Z",
      "location_count": 1,
      "location_summary": "Golden, Colorado",
      "locations": [
        {
          "city": "Golden",
          "state": "Colorado"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03122119"
    }
  ]
}