{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Sacroiliac+Joint&page=2",
    "query": {
      "condition": "Sacroiliac Joint",
      "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+Joint&page=1&page_size=10"
  },
  "source": "remote",
  "last_synced_at": "2026-06-10T22:58:56.226Z",
  "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": "NCT02373644",
      "title": "Spinal Manipulation and Dry Needling Versus Conventional Physical Therapy in Patients With Sacroiliac Dysfunction",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Sacroiliac Joint Dysfunction"
      ],
      "interventions": [
        {
          "name": "HVLA Thrust Manipulation and DN",
          "type": "OTHER"
        },
        {
          "name": "Conventional Physical Therapy",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "Alabama Physical Therapy & Acupuncture",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 116,
      "start_date": "2015-02-21",
      "completion_date": "2020-01-10",
      "has_results": false,
      "last_update_posted_date": "2020-02-19",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 1,
      "location_summary": "Montgomery, Alabama",
      "locations": [
        {
          "city": "Montgomery",
          "state": "Alabama"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02373644"
    },
    {
      "nct_id": "NCT05633888",
      "title": "Post-Market Feasibility Study of the Tenon Medical CATAMARAN™ SI Joint Fusion System",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Sacroiliac Joint Disruption",
        "Degenerative Sacroiliitis"
      ],
      "interventions": [
        {
          "name": "CATAMARAN SI Joint Fusion System",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Tenon Medical",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "75 Years",
        "sex": "ALL",
        "summary": "18 Years to 75 Years"
      },
      "enrollment_count": 50,
      "start_date": "2022-11-14",
      "completion_date": "2026-01",
      "has_results": false,
      "last_update_posted_date": "2024-03-20",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 6,
      "location_summary": "Coeur d'Alene, Idaho • Muncie, Indiana • Louisville, Kentucky + 3 more",
      "locations": [
        {
          "city": "Coeur d'Alene",
          "state": "Idaho"
        },
        {
          "city": "Muncie",
          "state": "Indiana"
        },
        {
          "city": "Louisville",
          "state": "Kentucky"
        },
        {
          "city": "Duluth",
          "state": "Minnesota"
        },
        {
          "city": "Chesterfield",
          "state": "Missouri"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05633888"
    },
    {
      "nct_id": "NCT03518840",
      "title": "Predictive Value of the Active Straight Leg Raise on the Efficacy of a SJB in Posterior PGP During Pregnancy",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Pelvic Girdle Pain"
      ],
      "interventions": [
        {
          "name": "SIJ Belt",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Loyola University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "50 Years",
        "sex": "FEMALE",
        "summary": "18 Years to 50 Years · Female only"
      },
      "enrollment_count": 63,
      "start_date": "2017-11-07",
      "completion_date": "2019-03-21",
      "has_results": true,
      "last_update_posted_date": "2020-11-24",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 1,
      "location_summary": "Maywood, Illinois",
      "locations": [
        {
          "city": "Maywood",
          "state": "Illinois"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03518840"
    },
    {
      "nct_id": "NCT02096653",
      "title": "Fluoroscopically-guided Versus Landmark-guided Sacroiliac Joint Injections",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Sacroiliac Joint Pain"
      ],
      "interventions": [
        {
          "name": "X-ray SI joint steroid injection",
          "type": "PROCEDURE"
        },
        {
          "name": "Landmark-guided SI steroid injection",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Johns Hopkins University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "100 Years",
        "sex": "ALL",
        "summary": "18 Years to 100 Years"
      },
      "enrollment_count": 125,
      "start_date": "2014-05",
      "completion_date": "2017-11",
      "has_results": false,
      "last_update_posted_date": "2018-02-07",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 4,
      "location_summary": "San Diego, California • Baltimore, Maryland • Rockville, Maryland + 1 more",
      "locations": [
        {
          "city": "San Diego",
          "state": "California"
        },
        {
          "city": "Baltimore",
          "state": "Maryland"
        },
        {
          "city": "Rockville",
          "state": "Maryland"
        },
        {
          "city": "Hershey",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02096653"
    },
    {
      "nct_id": "NCT01874236",
      "title": "Validity and Reliability of Diagnostic Findings of SI Joint Blocking",
      "overall_status": "TERMINATED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "SI Joint Pain"
      ],
      "interventions": [
        {
          "name": "0.75% bupivacaine",
          "type": "DRUG"
        },
        {
          "name": ".75% bupivacaine",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "SI-BONE, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": "75 Years",
        "sex": "ALL",
        "summary": "21 Years to 75 Years"
      },
      "enrollment_count": 28,
      "start_date": "2013-04-22",
      "completion_date": "2014-09-30",
      "has_results": false,
      "last_update_posted_date": "2019-09-24",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 7,
      "location_summary": "Mount Vernon, Illinois • Lexington, Kentucky • Cleveland, Ohio + 4 more",
      "locations": [
        {
          "city": "Mount Vernon",
          "state": "Illinois"
        },
        {
          "city": "Lexington",
          "state": "Kentucky"
        },
        {
          "city": "Cleveland",
          "state": "Ohio"
        },
        {
          "city": "Hershey",
          "state": "Pennsylvania"
        },
        {
          "city": "Tyler",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01874236"
    },
    {
      "nct_id": "NCT02808962",
      "title": "Optimal Performance of RFA of the Nerves Supplying the Posterior Sacroiliac Joint Complex.",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Osteoarthritis Nos, of Sacroiliac Joint"
      ],
      "interventions": [
        {
          "name": "Cooled RFA of sacral lateral branches",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Milton S. Hershey Medical Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 60,
      "start_date": "2016-02-17",
      "completion_date": "2022-06-01",
      "has_results": false,
      "last_update_posted_date": "2022-07-11",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 1,
      "location_summary": "Hershey, Pennsylvania",
      "locations": [
        {
          "city": "Hershey",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT02808962"
    },
    {
      "nct_id": "NCT03744234",
      "title": "Platelet-rich Plasma in the Sacroiliac Joint",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Sacroiliac Joint Arthritis"
      ],
      "interventions": [
        {
          "name": "PRP",
          "type": "PROCEDURE"
        },
        {
          "name": "Steroid Injection",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Columbia University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 40,
      "start_date": "2016-12-01",
      "completion_date": "2019-09-16",
      "has_results": false,
      "last_update_posted_date": "2019-09-18",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03744234"
    },
    {
      "nct_id": "NCT05409443",
      "title": "Conventional vs Bipolar SIJ RFA for Treatment of Sacroiliac Joint Pain",
      "overall_status": "RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Sacroiliac Joint Complex",
        "Low Back Pain"
      ],
      "interventions": [
        {
          "name": "Nimbus Sacroiliac Joint Radiofrequency Ablation (N-SIJRFA)",
          "type": "PROCEDURE"
        },
        {
          "name": "Conventional Sacroiliac Joint Radiofrequency Ablation (C-SIJRFA)",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "University of Utah",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "90 Years",
        "sex": "ALL",
        "summary": "18 Years to 90 Years"
      },
      "enrollment_count": 116,
      "start_date": "2022-08-15",
      "completion_date": "2027-06-30",
      "has_results": false,
      "last_update_posted_date": "2024-05-14",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 3,
      "location_summary": "Farmington, Utah • Salt Lake City, Utah • South Jordan, Utah",
      "locations": [
        {
          "city": "Farmington",
          "state": "Utah"
        },
        {
          "city": "Salt Lake City",
          "state": "Utah"
        },
        {
          "city": "South Jordan",
          "state": "Utah"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT05409443"
    },
    {
      "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": "2026-06-10T22:58:56.226Z",
      "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": "NCT00649753",
      "title": "Algometer and Category II Pelvic Blocking and Cranial Protocol",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Pain",
        "Sacroiliac Joint Dysfunction"
      ],
      "interventions": [
        {
          "name": "Category II Pelvic Blocking",
          "type": "PROCEDURE"
        },
        {
          "name": "Category II Pelvic Blocking and Cranial",
          "type": "PROCEDURE"
        },
        {
          "name": "Cranial Only",
          "type": "PROCEDURE"
        }
      ],
      "intervention_types": [
        "PROCEDURE"
      ],
      "sponsor": "Logan College of Chiropractic",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "60 Years",
        "sex": "ALL",
        "summary": "18 Years to 60 Years"
      },
      "enrollment_count": 40,
      "start_date": "2008-03",
      "completion_date": "2008-08",
      "has_results": false,
      "last_update_posted_date": "2009-07-23",
      "last_synced_at": "2026-06-10T22:58:56.226Z",
      "location_count": 1,
      "location_summary": "Chesterfield, Missouri",
      "locations": [
        {
          "city": "Chesterfield",
          "state": "Missouri"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00649753"
    }
  ]
}