{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Compression+Therapy&page=25", "query": { "intervention": "Compression Therapy", "page": 25 }, "page_size": 10 }, "pagination": { "page": 25, "page_size": 10, "total_count": 616, "total_pages": 62, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Compression+Therapy&page=26&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Compression+Therapy&page=24&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-27T01:48:24.144Z", "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": "NCT06549842", "title": "Safe and Fast Radial Hemostasis Using Synergistic Strategies: SAFE & FAST Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiovascular Diseases", "Bleeding", "Arterial Puncture", "Catheter Complications", "Occlusion of Artery" ], "interventions": [ { "name": "Heparin", "type": "DRUG" }, { "name": "Terumo Radial Band", "type": "DEVICE" }, { "name": "Vaosband", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "Regional Hospital of Scranton", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 451, "start_date": "2024-08-15", "completion_date": "2026-02-20", "has_results": false, "last_update_posted_date": "2026-03-03", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 1, "location_summary": "Scranton, Pennsylvania", "locations": [ { "city": "Scranton", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06549842" }, { "nct_id": "NCT01549860", "title": "Effects of Non Contact Low Frequency Ultrasound in Healing Venous Leg Ulcers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Venous Insufficiency", "Venous Reflux", "Lower Extremity Ulcer" ], "interventions": [ { "name": "MIST Therapy", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Celleration, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 156, "start_date": "2012-04", "completion_date": "2015-04", "has_results": true, "last_update_posted_date": "2015-07-30", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 1, "location_summary": "Weymouth, Massachusetts", "locations": [ { "city": "Weymouth", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01549860" }, { "nct_id": "NCT00290862", "title": "A Safety and Efficacy Study for Treatment of Painful Vertebral Compression Fractures Caused by Osteoporosis", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Fractures" ], "interventions": [ { "name": "Percutaneous Vertebral Augmentation of compression fractures", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Orthovita d/b/a Stryker", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 256, "start_date": "2004-09", "completion_date": "2009-03", "has_results": false, "last_update_posted_date": "2008-10-15", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 18, "location_summary": "Scottsdale, Arizona • Encinitas, California • Rancho Mirage, California + 14 more", "locations": [ { "city": "Scottsdale", "state": "Arizona" }, { "city": "Encinitas", "state": "California" }, { "city": "Rancho Mirage", "state": "California" }, { "city": "Santa Monica", "state": "California" }, { "city": "Vero Beach", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT00290862" }, { "nct_id": "NCT07397182", "title": "SleepSMART for Veterans With Insomnia and Mild Cognitive Impairment", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Insomnia", "Mild Cognitive Impairment" ], "interventions": [ { "name": "Cognitive BehavioralTherapy for Insomnia (CBT-I)", "type": "BEHAVIORAL" }, { "name": "SleepSMART", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 150, "start_date": "2026-11-02", "completion_date": "2030-03-31", "has_results": false, "last_update_posted_date": "2026-07-23", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07397182" }, { "nct_id": "NCT03250247", "title": "Chronic Venous Thrombosis: Relief With Adjunctive Catheter-Directed Therapy (The C-TRACT Trial)", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Deep Vein Thrombosis", "Venous Stasis", "Venous Insufficiency", "Venous Leg Ulcer", "Venous Reflux", "Post Thrombotic Syndrome" ], "interventions": [ { "name": "Stents", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 225, "start_date": "2018-07-02", "completion_date": "2026-04-27", "has_results": false, "last_update_posted_date": "2026-01-28", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 29, "location_summary": "Orange, California • San Francisco, California • New Haven, Connecticut + 23 more", "locations": [ { "city": "Orange", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "New Haven", "state": "Connecticut" }, { "city": "Newark", "state": "Delaware" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03250247" }, { "nct_id": "NCT02462226", "title": "Enhancing Management of Chronic Pain and Symptoms Among Women Treated for Breast Cancer (Lymph-Flow)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer", "Pain", "Lymphedema" ], "interventions": [ { "name": "The-Optimal-Lymph-Flow", "type": "BEHAVIORAL" }, { "name": "Arm Precaution", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "89 Years", "sex": "FEMALE", "summary": "21 Years to 89 Years · Female only" }, "enrollment_count": 120, "start_date": "2015-05-01", "completion_date": "2016-12-01", "has_results": false, "last_update_posted_date": "2017-04-20", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02462226" }, { "nct_id": "NCT01372748", "title": "Continuous Chest Compressions vs AHA Standard CPR of 30:2", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Out of Hospital Cardiac Arrest" ], "interventions": [ { "name": "Standard CPR", "type": "OTHER" }, { "name": "Continuous chest compressions", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 23711, "start_date": "2011-06", "completion_date": "2015-11", "has_results": true, "last_update_posted_date": "2016-12-28", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 5, "location_summary": "Birmingham, Alabama • Pittsburgh, Pennsylvania • Dallas, Texas + 2 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Pittsburgh", "state": "Pennsylvania" }, { "city": "Dallas", "state": "Texas" }, { "city": "Seattle", "state": "Washington" }, { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT01372748" }, { "nct_id": "NCT05911243", "title": "Feasibility of Auricular Acupressure for Appetite and Weight in Patients With Stage II-IV Gastric, Esophageal, and Pancreatic Cancer", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Clinical Stage II Esophageal Adenocarcinoma AJCC v8", "Clinical Stage II Esophageal Squamous Cell Carcinoma AJCC v8", "Clinical Stage II Gastric Cancer AJCC v8", "Clinical Stage III Esophageal Adenocarcinoma AJCC v8", "Clinical Stage III Esophageal Squamous Cell Carcinoma AJCC v8", "Clinical Stage III Gastric Cancer AJCC v8", "Clinical Stage IV Esophageal Adenocarcinoma AJCC v8", "Clinical Stage IV Esophageal Squamous Cell Carcinoma AJCC v8", "Clinical Stage IV Gastric Cancer AJCC v8", "Stage II Pancreatic Cancer AJCC v8", "Stage III Pancreatic Cancer AJCC v8", "Stage IV Pancreatic Cancer AJCC v8" ], "interventions": [ { "name": "Acupressure Therapy", "type": "PROCEDURE" }, { "name": "Best Practice", "type": "OTHER" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 3, "start_date": "2024-07-22", "completion_date": "2025-07-09", "has_results": false, "last_update_posted_date": "2026-05-18", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT05911243" }, { "nct_id": "NCT00787358", "title": "A Proof-of-Concept Study Investigating the Safety and Efficacy of ZT-031 on Hip Fracture Healing in Men and Postmenopausal Women", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Hip Fracture" ], "interventions": [ { "name": "ZT-031", "type": "DRUG" }, { "name": "placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Zelos Therapeutics", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": null, "sex": "ALL", "summary": "30 Years and older" }, "enrollment_count": 50, "start_date": "2008-12", "completion_date": "2009-07", "has_results": false, "last_update_posted_date": "2009-06-04", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 1, "location_summary": "Rochester, New York", "locations": [ { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00787358" }, { "nct_id": "NCT05226585", "title": "Mechanisms of Change in Cognitive Behavioral Therapy for Insomnia (CBTi)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Initiation and Maintenance Disorders" ], "interventions": [ { "name": "In-Person Cognitive Behavioral Therapy for Insomnia", "type": "BEHAVIORAL" }, { "name": "Telehealth Cognitive Behavioral Therapy for Insomnia", "type": "BEHAVIORAL" }, { "name": "Internet Cognitive Behavioral Therapy for Insomnia", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Arizona", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "50 Years to 65 Years" }, "enrollment_count": 93, "start_date": "2021-09-26", "completion_date": "2024-12-17", "has_results": false, "last_update_posted_date": "2025-04-16", "last_synced_at": "2026-10-27T01:48:24.144Z", "location_count": 1, "location_summary": "Tucson, Arizona", "locations": [ { "city": "Tucson", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT05226585" } ] }