{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Control+%28standard+practice%29&page=27", "query": { "intervention": "Control (standard practice)", "page": 27 }, "page_size": 10 }, "pagination": { "page": 27, "page_size": 10, "total_count": 971, "total_pages": 98, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Control+%28standard+practice%29&page=28&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Control+%28standard+practice%29&page=26&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-15T10:21:11.078Z", "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": "NCT04450693", "title": "Cryopreserved Human Umbilical Cord (TTAX01) for Late Stage, Complex Non-healing Diabetic Foot Ulcers (AMBULATE DFU II)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Diabetic Foot Infection", "Non-healing Wound", "Non-healing Diabetic Foot Ulcer" ], "interventions": [ { "name": "TTAX01", "type": "BIOLOGICAL" }, { "name": "Standard care", "type": "OTHER" } ], "intervention_types": [ "BIOLOGICAL", "OTHER" ], "sponsor": "BioTissue Holdings, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 106, "start_date": "2020-11-20", "completion_date": "2025-03-24", "has_results": false, "last_update_posted_date": "2025-04-01", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 16, "location_summary": "Guntersville, Alabama • Tucson, Arizona • Los Angeles, California + 12 more", "locations": [ { "city": "Guntersville", "state": "Alabama" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Los Angeles", "state": "California" }, { "city": "Mather", "state": "California" }, { "city": "Palmdale", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04450693" }, { "nct_id": "NCT03186430", "title": "PreTeenVax Evaluation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Human Papilloma Virus" ], "interventions": [ { "name": "Comprehensive Vaccine Promotion Package", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "11 Years", "maximum_age": "12 Years", "sex": "ALL", "summary": "11 Years to 12 Years" }, "enrollment_count": 168, "start_date": "2017-06-14", "completion_date": "2018-07-31", "has_results": false, "last_update_posted_date": "2018-08-08", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 6, "location_summary": "Canton, Georgia • Duluth, Georgia • Lawrenceville, Georgia + 3 more", "locations": [ { "city": "Canton", "state": "Georgia" }, { "city": "Duluth", "state": "Georgia" }, { "city": "Lawrenceville", "state": "Georgia" }, { "city": "Lithia Springs", "state": "Georgia" }, { "city": "Loganville", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03186430" }, { "nct_id": "NCT04875052", "title": "Vibration and Post-traumatic Osteoarthritis Risk Following ACL Injury", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis, Knee", "Anterior Cruciate Ligament Injuries", "Post-traumatic Osteoarthritis", "Quadriceps Muscle Atrophy" ], "interventions": [ { "name": "Experimental: Whole Body Vibration", "type": "DEVICE" }, { "name": "Experimental: Local Muscle Vibration", "type": "DEVICE" }, { "name": "Standard ACL Rehabilitation", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "16 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "16 Years to 35 Years" }, "enrollment_count": 114, "start_date": "2021-01-11", "completion_date": "2026-08", "has_results": false, "last_update_posted_date": "2025-05-31", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 2, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" }, { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04875052" }, { "nct_id": "NCT05436392", "title": "De-adopting Routine Preoperative Benzodiazepines for Older Surgical Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgery", "Aging" ], "interventions": [ { "name": "Peer Comparison Feedback", "type": "BEHAVIORAL" }, { "name": "Patient Informational Letter", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 517611, "start_date": "2022-08-08", "completion_date": "2023-12-31", "has_results": false, "last_update_posted_date": "2024-01-18", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05436392" }, { "nct_id": "NCT02052284", "title": "The Application of Sterile Water to the Skin of Extremely Low Birth Weight (ELBW) Infants", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Fluid Loss", "Dehydration", "Extreme Immaturity" ], "interventions": [ { "name": "Sterile water application", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "24 Hours", "sex": "ALL", "summary": "Up to 24 Hours" }, "enrollment_count": 30, "start_date": "2014-01", "completion_date": "2017-12-31", "has_results": false, "last_update_posted_date": "2018-01-23", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02052284" }, { "nct_id": "NCT03887299", "title": "Antimicrobial Dressing Versus Standard Dressing in Obese Women Undergoing Cesarean Delivery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cesarean Section Complications", "Wound Breakdown", "Wound Infection", "Satisfaction", "Surgical Wound Infection" ], "interventions": [ { "name": "ReliaTect™ Post-Op Dressing (contains chlorohexidine gluconate or CHG)", "type": "COMBINATION_PRODUCT" }, { "name": "Standard Wound Care", "type": "OTHER" } ], "intervention_types": [ "COMBINATION_PRODUCT", "OTHER" ], "sponsor": "The University of Texas Medical Branch, Galveston", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 154, "start_date": "2019-04-18", "completion_date": "2020-02-28", "has_results": true, "last_update_posted_date": "2021-10-05", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 1, "location_summary": "Galveston, Texas", "locations": [ { "city": "Galveston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03887299" }, { "nct_id": "NCT02037139", "title": "Hearing Health Care Service Access and Use", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hearing Loss" ], "interventions": [ { "name": "Screening", "type": "OTHER" }, { "name": "Brochure", "type": "OTHER" }, { "name": "Education", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 155, "start_date": "2013-07", "completion_date": "2019-09-15", "has_results": false, "last_update_posted_date": "2019-11-13", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02037139" }, { "nct_id": "NCT06855706", "title": "An Automated Personalized Physical Activity Intervention to Improve Immune Function and Clinical Outcomes in Stage II-IV Ovarian, Primary Peritoneal or Fallopian Tube Cancer and Newly Diagnosed Endometrial Cancer, Life on the Go 3 Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Endometrial Carcinoma", "Recurrent Fallopian Tube Carcinoma", "Recurrent Ovarian Carcinoma", "Recurrent Primary Peritoneal Carcinoma", "Stage II Fallopian Tube Cancer AJCC v8", "Stage II Ovarian Cancer AJCC v8", "Stage II Primary Peritoneal Cancer AJCC v8", "Stage III Fallopian Tube Cancer AJCC v8", "Stage III Ovarian Cancer AJCC v8", "Stage III Primary Peritoneal Cancer AJCC v8", "Stage IV Fallopian Tube Cancer AJCC v8", "Stage IV Ovarian Cancer AJCC v8", "Stage IV Primary Peritoneal Cancer AJCC v8" ], "interventions": [ { "name": "Behavioral Intervention", "type": "BEHAVIORAL" }, { "name": "Best Practice", "type": "OTHER" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Electronic Health Record Review", "type": "OTHER" }, { "name": "Exercise Intervention", "type": "OTHER" }, { "name": "Medical Device Usage and Evaluation", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Supportive Care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER", "PROCEDURE" ], "sponsor": "Roswell Park Cancer Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2025-06-04", "completion_date": "2028-04-30", "has_results": false, "last_update_posted_date": "2026-01-06", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 1, "location_summary": "Buffalo, New York", "locations": [ { "city": "Buffalo", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06855706" }, { "nct_id": "NCT07227337", "title": "Being Safe, Healthy, And Positively Empowered (BSHAPE) Intervention Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post Traumatic Stress Disorder", "Depression", "Violence" ], "interventions": [ { "name": "BSHAPE", "type": "BEHAVIORAL" }, { "name": "Control (general wellness)", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Johns Hopkins University", "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": 676, "start_date": "2025-11-05", "completion_date": "2028-12-31", "has_results": false, "last_update_posted_date": "2026-05-06", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT07227337" }, { "nct_id": "NCT01070056", "title": "Practice-based Trial of Blood Pressure Control in African Americans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Hypertension", "Physical Activity", "Diet", "Medication Adherence" ], "interventions": [ { "name": "Therapeutic Lifestyle Changes (MINT-TLC)", "type": "BEHAVIORAL" }, { "name": "Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 194, "start_date": "2010-02", "completion_date": "2012-07", "has_results": false, "last_update_posted_date": "2013-11-13", "last_synced_at": "2026-11-15T10:21:11.078Z", "location_count": 4, "location_summary": "Brooklyn, New York • New York, New York", "locations": [ { "city": "Brooklyn", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01070056" } ] }