{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Operative+Data&page=8", "query": { "intervention": "Operative Data", "page": 8 }, "page_size": 10 }, "pagination": { "page": 8, "page_size": 10, "total_count": 363, "total_pages": 37, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Operative+Data&page=9&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Operative+Data&page=7&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-06T23:52:24.883Z", "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": "NCT07106541", "title": "Population Based Strategies for Standardized Surgical Care", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hernia, Abdominal" ], "interventions": [ { "name": "Replicating Effective Programs (REP)", "type": "BEHAVIORAL" }, { "name": "REP with facilitation (REP-PLUS)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 68, "start_date": "2026-06", "completion_date": "2029-06", "has_results": false, "last_update_posted_date": "2025-08-06", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT07106541" }, { "nct_id": "NCT01045499", "title": "LAGB as a Treatment for Morbid Obesity in Adolescents", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Morbid Obesity", "Obstructive Sleep Apnea Syndrome", "Metabolic Syndrome", "Insulin Resistance", "Nonalcoholic Fatty Liver Disease" ], "interventions": [ { "name": "Laparoscopic adjustable gastric banding (Allergan Lap Band)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Jeffrey L Zitsman, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": "19 Years", "sex": "ALL", "summary": "13 Years to 19 Years" }, "enrollment_count": 137, "start_date": "2005-09-13", "completion_date": "2017-04-30", "has_results": true, "last_update_posted_date": "2020-04-13", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01045499" }, { "nct_id": "NCT07588698", "title": "Epcoritamab in Combination With R-CHOP for Patients With Aggressive Non-Hodgkin Lymphoma", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Non-Hodgkin's B-cell Lymphoma", "Lymphoma Non-Hodgkin", "Diffuse Large B-Cell Lymphoma (DLBCL)" ], "interventions": [ { "name": "Rituximab, Cyclophosphamide, Hydroxydaunorubicin, Oncovin, Prednisolone (R-CHOP)", "type": "DRUG" }, { "name": "Epcoritamab", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Positron Emission Tomography (PET)", "type": "PROCEDURE" }, { "name": "Blood specimen collection", "type": "PROCEDURE" }, { "name": "Questionnaires", "type": "BEHAVIORAL" }, { "name": "Computerized tomography (CT)", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE", "BEHAVIORAL" ], "sponsor": "Carrie Ho, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2026-11-15", "completion_date": "2029-08-31", "has_results": false, "last_update_posted_date": "2026-10-01", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 2, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07588698" }, { "nct_id": "NCT02345629", "title": "Cordotomy for Refractory Cancer Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Advanced Cancers", "Pain" ], "interventions": [ { "name": "Cordotomy", "type": "PROCEDURE" }, { "name": "Pain/Symptom Questionnaire", "type": "BEHAVIORAL" }, { "name": "Sharpness Sensory Testing", "type": "PROCEDURE" }, { "name": "Heat Pain Sensory Testing", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "BEHAVIORAL" ], "sponsor": "M.D. Anderson Cancer Center", "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": "2015-03-10", "completion_date": "2020-02-25", "has_results": false, "last_update_posted_date": "2023-06-07", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02345629" }, { "nct_id": "NCT03887520", "title": "Lipoprotein(a) in Patients With Cardiovascular Disease (CVD)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiovascular Disease and Lipoprotein(a)" ], "interventions": [ { "name": "Blood draw for Lp(a)", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Novartis Pharmaceuticals", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 49001, "start_date": "2018-11-27", "completion_date": "2021-07-30", "has_results": false, "last_update_posted_date": "2022-01-28", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 180, "location_summary": "Andalusia, Alabama • Birmingham, Alabama • Huntsville, Alabama + 150 more", "locations": [ { "city": "Andalusia", "state": "Alabama" }, { "city": "Birmingham", "state": "Alabama" }, { "city": "Huntsville", "state": "Alabama" }, { "city": "Mobile", "state": "Alabama" }, { "city": "Cottonwood", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT03887520" }, { "nct_id": "NCT06101303", "title": "Endometriosis Pain", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Pelvic Pain", "Endometriosis" ], "interventions": [ { "name": "Psychophysical assessment", "type": "OTHER" }, { "name": "Psychophysical assessments of experimental pain", "type": "BEHAVIORAL" }, { "name": "Blood, urine and saliva samples", "type": "DIAGNOSTIC_TEST" }, { "name": "Biopsy and surgery-related data.", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "BEHAVIORAL", "DIAGNOSTIC_TEST", "PROCEDURE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "12 Years to 45 Years · Female only" }, "enrollment_count": 120, "start_date": "2023-09-29", "completion_date": "2029-09-01", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT06101303" }, { "nct_id": "NCT07036926", "title": "Video-Based AI-Generated Peri-operative Instructions for Mitral Valve Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mitral Valve Repair Surgery" ], "interventions": [ { "name": "Artificial Intelligence Video Education Arm", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Joanna Chikwe", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2025-08-01", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-02-25", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07036926" }, { "nct_id": "NCT01184183", "title": "Trial Comparison of Accuseal and Bovine Pericardial Patch During Endarterectomy", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Coronary Stenosis" ], "interventions": [ { "name": "Comparing Accuseal Vs. Bovine Pericardial in CEA", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "CAMC Health System", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 200, "start_date": "2009-09", "completion_date": "2012-01", "has_results": false, "last_update_posted_date": "2026-08-18", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "Charleston, West Virginia", "locations": [ { "city": "Charleston", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01184183" }, { "nct_id": "NCT03906942", "title": "Team Science to Promote Physical Activity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Health Promotion" ], "interventions": [ { "name": "Fun For Wellness (FFW)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Michigan State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 33, "start_date": "2019-11-07", "completion_date": "2020-04-02", "has_results": false, "last_update_posted_date": "2020-09-02", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "East Lansing, Michigan", "locations": [ { "city": "East Lansing", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03906942" }, { "nct_id": "NCT04306939", "title": "Genomic Resources for Enhancing Available Therapies (GREAT1.0) Study", "overall_status": "SUSPENDED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Chronic Pancreatitis", "Inflammatory Bowel Diseases", "Hepatitis", "NASH - Nonalcoholic Steatohepatitis", "Acute Pancreatitis", "Rheumatoid Arthritis", "Diabetes Mellitus", "Dyslipidemias", "Multiple Sclerosis", "Irritable Bowel Syndrome", "Chronic Pain", "Chronic Disease", "Chronic Kidney Diseases", "Crohn Disease", "Celiac Disease", "Biliary Cirrhosis", "Bile Acid Synthesis Defect", "Gastritis", "Cholecystitis", "Cholelithiases", "IPMN", "Cyst Pancreas", "Cystic Fibrosis", "Pancreatic Exocrine Insufficiency", "Diarrhea Chronic", "Constipation - Functional", "Constipation Chronic Idiopathic" ], "interventions": [ { "name": "venipuncture", "type": "OTHER" }, { "name": "Questionnaires", "type": "BEHAVIORAL" }, { "name": "Additional Sample Collections", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": null, "sex": "ALL", "summary": "12 Years and older" }, "enrollment_count": 120000, "start_date": "2014-11-01", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-01-07", "last_synced_at": "2026-11-06T23:52:24.883Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04306939" } ] }