{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Non-operative+intervention&page=63", "query": { "intervention": "Non-operative intervention", "page": 63 }, "page_size": 10 }, "pagination": { "page": 63, "page_size": 10, "total_count": 1612, "total_pages": 162, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Non-operative+intervention&page=64&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Non-operative+intervention&page=62&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-24T06:24:52.637Z", "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": "NCT00486512", "title": "Chemoprevention of Colorectal Adenomas", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Adenomatous Polyps" ], "interventions": [ { "name": "0.5 mg calcitriol (1a -25-dihydroxycholecalciferol)", "type": "DRUG" }, { "name": "75 mg acetylsalicylic acid (ASA) + 1250 mg calcium carbonate (CaCO3)", "type": "DRUG" }, { "name": "placebo to 0.5 mg calcitriol (1a -25-dihydroxycholecalciferol)", "type": "DRUG" }, { "name": "placebo to 75 mg acetylsalicylic acid (ASA) + 1250 mg calcium carbonate (CaCO3)", "type": "DRUG" }, { "name": "Colonoscopy", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "Colotech A/S", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "40 Years to 75 Years" }, "enrollment_count": 350, "start_date": "2007-06", "completion_date": "2010-11", "has_results": false, "last_update_posted_date": "2020-09-03", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 24, "location_summary": "Huntsville, Alabama • San Diego, California • Clearwater, Florida + 20 more", "locations": [ { "city": "Huntsville", "state": "Alabama" }, { "city": "San Diego", "state": "California" }, { "city": "Clearwater", "state": "Florida" }, { "city": "Orlando", "state": "Florida" }, { "city": "Decatur", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT00486512" }, { "nct_id": "NCT01480167", "title": "The PRIORi-T Trial--Prospective Randomized Investigation of Radiofrequency Targeted Vertebral Augmentation", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Painful Osteoporotic Vertebral Compression Fractures (VCF)" ], "interventions": [ { "name": "Vertebral Augmentation (STABILIT)", "type": "DEVICE" }, { "name": "Non-operative Management", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "DFINE Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "21 Years to 90 Years" }, "enrollment_count": 0, "start_date": "2011-11", "completion_date": null, "has_results": false, "last_update_posted_date": "2017-01-20", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 6, "location_summary": "St Louis, Missouri • Lebanon, New Hampshire • Mineola, New York + 3 more", "locations": [ { "city": "St Louis", "state": "Missouri" }, { "city": "Lebanon", "state": "New Hampshire" }, { "city": "Mineola", "state": "New York" }, { "city": "The Bronx", "state": "New York" }, { "city": "Hershey", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01480167" }, { "nct_id": "NCT06477965", "title": "Embo Registry; National Registry for Artery Embolization", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Chronic Pain", "Osteoarthritis, Knee", "Osteoarthritis Thumb", "Osteoarthritis Shoulder", "Pain, Chronic", "Tendonitis Elbow", "Tendonitis Shoulder", "Tendonitis;Achilles", "Tenosynovitis" ], "interventions": [ { "name": "Artery Embolization", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Vascular Solutions of North Carolina", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1000, "start_date": "2024-07-15", "completion_date": "2029-07-15", "has_results": false, "last_update_posted_date": "2024-10-28", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 2, "location_summary": "Cary, North Carolina • Winchester, Tennessee", "locations": [ { "city": "Cary", "state": "North Carolina" }, { "city": "Winchester", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT06477965" }, { "nct_id": "NCT00058292", "title": "Radiolabeled Monoclonal Antibody Therapy and High-Dose Chemotherapy Followed By Autologous Peripheral Stem Cell Transplant in Treating Patients With Relapsed or Refractory Non-Hodgkin's Lymphoma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Lymphoma" ], "interventions": [ { "name": "filgrastim", "type": "BIOLOGICAL" }, { "name": "rituximab", "type": "BIOLOGICAL" }, { "name": "Carmustine", "type": "DRUG" }, { "name": "cytarabine", "type": "DRUG" }, { "name": "etoposide", "type": "DRUG" }, { "name": "melphalan", "type": "DRUG" }, { "name": "peripheral blood stem cell transplantation", "type": "PROCEDURE" }, { "name": "yttrium Y 90 ibritumomab tiuxetan", "type": "RADIATION" } ], "intervention_types": [ "BIOLOGICAL", "DRUG", "PROCEDURE", "RADIATION" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "17 Years", "maximum_age": null, "sex": "ALL", "summary": "17 Years and older" }, "enrollment_count": 44, "start_date": "2000-04", "completion_date": "2009-03", "has_results": false, "last_update_posted_date": "2012-06-01", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 3, "location_summary": "Chicago, Illinois • Rochester, Minnesota", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT00058292" }, { "nct_id": "NCT07148895", "title": "Assessing Post-operative Outcomes After Children's Sistrunk Procedure With or Without a Drain", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Thyroglossal Duct Cysts" ], "interventions": [ { "name": "Post-surgical drain", "type": "PROCEDURE" }, { "name": "No post-surgical drain", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Rochester", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "3 Years to 17 Years" }, "enrollment_count": 178, "start_date": "2026-01-09", "completion_date": "2029-12-31", "has_results": false, "last_update_posted_date": "2026-09-09", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 5, "location_summary": "Los Angeles, California • Hartford, Connecticut • Chicago, Illinois + 2 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Hartford", "state": "Connecticut" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07148895" }, { "nct_id": "NCT04804137", "title": "Immune Response Under Immunotherapy in Metastatic NSCLC: Sputum, Blood Samples and Microbioata Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Non-squamous Lung Cancer", "Metastatic Lung Cancer" ], "interventions": [ { "name": "Blood", "type": "OTHER" }, { "name": "sputum", "type": "OTHER" }, { "name": "saliva", "type": "OTHER" }, { "name": "stool", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University Hospital, Tours", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 24, "start_date": "2021-05-03", "completion_date": "2023-07-31", "has_results": false, "last_update_posted_date": "2024-01-17", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04804137" }, { "nct_id": "NCT02017145", "title": "Study on the Reapplication of Chloraprep After Lower Extremity Surgery and Prior to Dressing Application", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Lower Extremity Surgery", "Surgical Site Infection", "Bacterial Colonization", "Surgical Antiseptic" ], "interventions": [ { "name": "Chloraprep", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Sanford Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 140, "start_date": "2014-02", "completion_date": null, "has_results": false, "last_update_posted_date": "2014-02-19", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 1, "location_summary": "Sioux Falls, South Dakota", "locations": [ { "city": "Sioux Falls", "state": "South Dakota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02017145" }, { "nct_id": "NCT05796375", "title": "Replacing Invasive Cystoscopy With Urine Testing for Non-muscle Invasive Bladder Cancer Surveillance", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Non-muscle-invasive Bladder Cancer" ], "interventions": [ { "name": "Cystoscopy", "type": "PROCEDURE" }, { "name": "Bladder EpiCheck urine test", "type": "DIAGNOSTIC_TEST" }, { "name": "Xpert Bladder Cancer Monitor urine test", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "PROCEDURE", "DIAGNOSTIC_TEST" ], "sponsor": "White River Junction Veterans Affairs Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 240, "start_date": "2023-11-17", "completion_date": "2028-12-30", "has_results": false, "last_update_posted_date": "2026-09-16", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 10, "location_summary": "West Haven, Connecticut • Bay Pines, Florida • Tampa, Florida + 7 more", "locations": [ { "city": "West Haven", "state": "Connecticut" }, { "city": "Bay Pines", "state": "Florida" }, { "city": "Tampa", "state": "Florida" }, { "city": "West Roxbury", "state": "Massachusetts" }, { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05796375" }, { "nct_id": "NCT04329494", "title": "PIPAC for the Treatment of Peritoneal Carcinomatosis in Patients With Ovarian, Uterine, Appendiceal, Colorectal, or Gastric Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Clinical Stage IV Gastric Cancer AJCC v8", "Clinical Stage IVA Gastric Cancer AJCC v8", "Clinical Stage IVB Gastric Cancer AJCC v8", "Malignant Uterine Neoplasm", "Metastatic Appendix Carcinoma", "Metastatic Colorectal Carcinoma", "Metastatic Gastric Carcinoma", "Metastatic Malignant Neoplasm in the Peritoneum", "Metastatic Malignant Solid Neoplasm", "Metastatic Ovarian Carcinoma", "Pathologic Stage IV Gastric Cancer AJCC v8", "Peritoneal Carcinomatosis", "Postneoadjuvant Therapy Stage IV Gastric Cancer AJCC v8", "Stage IV Appendix Carcinoma AJCC v8", "Stage IV Colorectal Cancer AJCC v8", "Stage IV Ovarian Cancer AJCC v8", "Stage IV Uterine Corpus Cancer AJCC v8", "Stage IVA Appendix Carcinoma AJCC v8", "Stage IVA Colorectal Cancer AJCC v8", "Stage IVA Ovarian Cancer AJCC v8", "Stage IVA Uterine Corpus Cancer AJCC v8", "Stage IVB Appendix Carcinoma AJCC v8", "Stage IVB Colorectal Cancer AJCC v8", "Stage IVB Ovarian Cancer AJCC v8", "Stage IVB Uterine Corpus Cancer AJCC v8", "Stage IVC Appendix Carcinoma AJCC v8", "Stage IVC Colorectal Cancer AJCC v8" ], "interventions": [ { "name": "Biopsy", "type": "PROCEDURE" }, { "name": "Cisplatin", "type": "DRUG" }, { "name": "Doxorubicin", "type": "DRUG" }, { "name": "Fluorouracil", "type": "DRUG" }, { "name": "Intraperitoneal Chemotherapy", "type": "DEVICE" }, { "name": "Irinotecan", "type": "DRUG" }, { "name": "Leucovorin", "type": "DRUG" }, { "name": "Mitomycin", "type": "DRUG" }, { "name": "Oxaliplatin", "type": "DRUG" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "DRUG", "DEVICE", "OTHER" ], "sponsor": "City of Hope 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": 49, "start_date": "2020-08-21", "completion_date": "2028-01-05", "has_results": false, "last_update_posted_date": "2026-08-26", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 3, "location_summary": "Duarte, California • Jacksonville, Florida • Greenlawn, New York", "locations": [ { "city": "Duarte", "state": "California" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Greenlawn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04329494" }, { "nct_id": "NCT07821931", "title": "Suzetrigine in Tonsillectomy for Opioid-sparing Pain Management", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Tonsillectomy", "Pharyngoplasty", "Suzetrigine", "Opioid", "Postoperative Pain", "Acute Pain" ], "interventions": [ { "name": "Suzetrigine", "type": "DRUG" }, { "name": "Acetaminophen", "type": "DRUG" }, { "name": "oxycodone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 58, "start_date": "2026-11", "completion_date": "2027-07", "has_results": false, "last_update_posted_date": "2026-09-16", "last_synced_at": "2026-10-24T06:24:52.637Z", "location_count": 1, "location_summary": "Palo Alto, California", "locations": [ { "city": "Palo Alto", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07821931" } ] }