{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=sutures&page=2", "query": { "intervention": "sutures", "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?intervention=sutures&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-16T15:32:32.894Z", "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": "NCT02923362", "title": "Registry of Outcomes From AntiReflux Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Gastroesophageal Reflux Disease", "Hiatal Hernia" ], "interventions": [ { "name": "Laparoscopic Fundoplication", "type": "PROCEDURE" }, { "name": "LINX Antireflux", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DEVICE" ], "sponsor": "The Heartburn Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 1941, "start_date": "2016-05", "completion_date": "2023-05-03", "has_results": false, "last_update_posted_date": "2026-08-07", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 19, "location_summary": "Birmingham, Alabama • Mobile, Alabama • Heber Springs, Arkansas + 15 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Mobile", "state": "Alabama" }, { "city": "Heber Springs", "state": "Arkansas" }, { "city": "Walnut Creek", "state": "California" }, { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT02923362" }, { "nct_id": "NCT03529162", "title": "A Prospective Study Comparing Suture Anchor and Soft Tissue Pectoralis Major Tendon Techniques for Biceps Tenodesis", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bicep Tendinitis", "Biceps; Tenosynovitis", "Biceps Tendon Disorder" ], "interventions": [ { "name": "Long head of Biceps Tenodesis", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "St. Louis University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 4, "start_date": "2018-10-19", "completion_date": "2020-01-27", "has_results": true, "last_update_posted_date": "2021-04-29", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 3, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" }, { "city": "St Louis", "state": "Missouri" }, { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03529162" }, { "nct_id": "NCT04982653", "title": "Short Stitch Versus Traditional Suture for the Prevention of Incisional Hernia After Open Hepatectomy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Liver and Intrahepatic Bile Duct Neoplasm", "Metastatic Malignant Neoplasm in the Liver", "Primary Malignant Liver Neoplasm" ], "interventions": [ { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Surgical Procedure", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "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": 140, "start_date": "2022-01-04", "completion_date": "2027-02-02", "has_results": false, "last_update_posted_date": "2026-05-26", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04982653" }, { "nct_id": "NCT06567691", "title": "Endoscopic Gastroenterostomy Versus Surgical Gastrojejunostomy", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Malignant Gastric Outlet Obstruction" ], "interventions": [ { "name": "EUS Gastrojejunostomy", "type": "PROCEDURE" }, { "name": "Surgical Gastrojejunostomy", "type": "PROCEDURE" }, { "name": "Gastric Outlet Obstruction Scoring System (GOOSS)", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Vanderbilt University 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": 34, "start_date": "2025-08-01", "completion_date": "2027-01", "has_results": false, "last_update_posted_date": "2025-08-26", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT06567691" }, { "nct_id": "NCT05729542", "title": "Comparing Clinical Outcomes of Suture Button Versus Fibulink Fixation for Acute Ankle Syndesmosis Injuries", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Ankle Injuries", "Syndesmotic Injuries", "Ankle Fractures" ], "interventions": [ { "name": "Arthrex Tightrope", "type": "DEVICE" }, { "name": "Synthes Fibulink", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 140, "start_date": "2021-11-18", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-02-10", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05729542" }, { "nct_id": "NCT05939973", "title": "A Feasibility Study for the Treatment of Primary Obesity Cross-over Arm", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity, Primary" ], "interventions": [ { "name": "g-Cath EZ Delivery Catheter with Snowshoe Suture Anchors", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "USGI Medical", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "22 Years to 60 Years" }, "enrollment_count": 3, "start_date": "2023-01-19", "completion_date": "2024-06-14", "has_results": false, "last_update_posted_date": "2026-05-15", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05939973" }, { "nct_id": "NCT01070069", "title": "Percutaneous Endovascular Aneurysm Repair (PEVAR) Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Abdominal Aortic Aneurysm" ], "interventions": [ { "name": "PEVAR (ProGlide closure)", "type": "DEVICE" }, { "name": "SEVAR (IntuiTrak)", "type": "DEVICE" }, { "name": "PEVAR (Prostar XL closure)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Endologix", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 192, "start_date": "2010-04-13", "completion_date": "2012-09-05", "has_results": true, "last_update_posted_date": "2022-06-07", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 20, "location_summary": "Loma Linda, California • San Diego, California • Fort Lauderdale, Florida + 15 more", "locations": [ { "city": "Loma Linda", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "Fort Lauderdale", "state": "Florida" }, { "city": "Gainesville", "state": "Florida" }, { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01070069" }, { "nct_id": "NCT01608568", "title": "Affixing Polypropylene Mesh Using Barbed Suture (Quill™ SRS) During Robotic Assisted Laparoscopic Sacrocolpopexy", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prolapse" ], "interventions": [ { "name": "Device is the type of suture used: Quill suture vs. Interrupted suture", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 32, "start_date": "2010-11", "completion_date": "2013-08", "has_results": false, "last_update_posted_date": "2012-06-01", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01608568" }, { "nct_id": "NCT07637838", "title": "Characterizing the Effects of Platelet-Rich Fibrin (PRF) as a Palatal Wound Dressing on Quality of Life and Sleep Following Mucogingival Surgery. Study Was Conducted at the Air Force Post Graduate Dental School. All HIPPA Consents and Research Informed Consents Are Located at JBSA-Lackland.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Palatal Donor Site Wound Healing", "Platelet Rich Fibrin", "Sleep Quality", "Pain", "Analgesic Consumption" ], "interventions": [ { "name": "Platelet rich fibrin", "type": "PROCEDURE" }, { "name": "Control Group: collagen matrices or oxidized cellulose membrane", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "59th Medical Wing", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 78, "start_date": "2024-05-24", "completion_date": "2025-03-18", "has_results": false, "last_update_posted_date": "2026-06-10", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07637838" }, { "nct_id": "NCT03814044", "title": "PMCF Study on PEEK Suture Anchors for Hip Indications", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Soft Tissue to Bone Fixation" ], "interventions": [ { "name": "PEEK Suture Anchors", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Smith & Nephew, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 149, "start_date": "2019-05-10", "completion_date": "2019-09-10", "has_results": true, "last_update_posted_date": "2024-10-15", "last_synced_at": "2026-09-16T15:32:32.894Z", "location_count": 4, "location_summary": "West Des Moines, Iowa • Auburn Hills, Michigan • Oklahoma City, Oklahoma", "locations": [ { "city": "West Des Moines", "state": "Iowa" }, { "city": "Auburn Hills", "state": "Michigan" }, { "city": "Oklahoma City", "state": "Oklahoma" }, { "city": "Oklahoma City", "state": "Oklahoma" } ], "official_url": "https://clinicaltrials.gov/study/NCT03814044" } ] }