{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Fracture+Repair&page=2", "query": { "condition": "Fracture Repair", "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?condition=Fracture+Repair&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-22T06:34:22.086Z", "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": "NCT02482727", "title": "BFR DISTRAD: Blood Flow Restricted Training During Rehabilitation Following Distal Radius Fracture Repair", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Distal Radius Fracture", "Rehabilitation" ], "interventions": [ { "name": "occlusion training with tourniquet (DELFI PTS ii portable tourniquet system)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Brooke Army Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 52, "start_date": "2015-06", "completion_date": null, "has_results": false, "last_update_posted_date": "2017-02-23", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02482727" }, { "nct_id": "NCT07004764", "title": "Enhancing Wound Perfusion in High-Risk Lower Extremity Orthopaedic Surgery: A Study on Nitropaste Using Intraoperative SPY Imaging.", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Achilles Tendon Repairs/Reconstructions", "Pilon Fracture of Tibia", "Tibial Plateau Fracture", "Ankle Fracture (Bimalleolar Equivalent, Bimalleolar, or Trimalleolar)", "Calcaneus Fractures", "Talus Fracture", "Wound Infection Deep", "Wound Infection Post-Traumatic", "Wound Dehiscence, Surgical" ], "interventions": [ { "name": "Nitroglycerin Ointment 2%", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15, "start_date": "2026-11", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-03-31", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 2, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" }, { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT07004764" }, { "nct_id": "NCT05584553", "title": "PMCF Study on the Safety, Performance and Clinical Benefits Data of the ToggleLoc™ 2.9mm and JuggerLoc™ in the Shoulder", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Bankart Lesions", "SLAP Lesion", "Acromioclavicular; Dislocation", "Capsular Shift/Capsulolabral Reconstruction", "Deltoid Repair", "Rotator Cuff Tear Repair", "Biceps Tendon Disorder" ], "interventions": [ { "name": "ToggleLoc 2.9 mm soft tissue device", "type": "DEVICE" }, { "name": "JuggerLoc soft tissue device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Zimmer Biomet", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 214, "start_date": "2022-12-02", "completion_date": "2024-06-30", "has_results": true, "last_update_posted_date": "2025-11-28", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "City of Saint Peters, Missouri", "locations": [ { "city": "City of Saint Peters", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05584553" }, { "nct_id": "NCT05062265", "title": "Internal Brace Augmented Anterior Inferior Tibiofibular Ligament Repair: Post-operative Syndesmotic Volumes.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Syndesmotic Injuries", "Ligament Rupture", "Bimalleolar Fractures", "Trimalleolar Fractures" ], "interventions": [ { "name": "Tight rope fixation", "type": "DEVICE" }, { "name": "Tight rope fixation with an anterior inferior tibiofibular ligament (AITFL) repair augmentation with an internal brace", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Vann Virginia Center for Orthopaedics dba Atlantic Orthopaedic Specialists", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 23, "start_date": "2022-01-31", "completion_date": "2023-12-31", "has_results": true, "last_update_posted_date": "2025-02-19", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "Virginia Beach, Virginia", "locations": [ { "city": "Virginia Beach", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05062265" }, { "nct_id": "NCT04715139", "title": "Evaluate the Continued Safety and Performance of the Foot and Ankle Products", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Hyperpronated Foot", "Reconstruction Surgeries of the Foot", "Fixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/Ankle", "Fixation of Small Bone Fragments of the Foot/Ankle", "Lisfranc Arthrodesis", "Mono or Bi-cortical Osteotomies in the Forefoot", "First Metatarsophalangeal Arthrodesis", "Akin Osteotomy", "Midfoot and Hindfoot Arthrodeses or Osteotomies", "Fixation of Osteotomies for Hallux Valgus Treatment (Scarf and Chevron)", "Arthrodesis of the Metatarsocuneiform Joint to Reposition and Stabilize Metatarsus Primus Varus", "Osteotomy Fixation of Hallux Valgus Repair (Such as Scarf and Chevron Etc.)", "Medial Ankle Stabilization", "Tibiotalocalcaneal Arthrodesis" ], "interventions": [ { "name": "Products listed in Group/Cohort Description", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Arthrex, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 700, "start_date": "2020-12-01", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-02-11", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 5, "location_summary": "Sacramento, California • Chicago, Illinois • Nashville, Tennessee + 2 more", "locations": [ { "city": "Sacramento", "state": "California" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Nashville", "state": "Tennessee" }, { "city": "San Antonio", "state": "Texas" }, { "city": "Virginia Beach", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04715139" }, { "nct_id": "NCT02604459", "title": "Does Optimized General Anesthesia Care Reduce Postoperative Delirium?", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hip Fractures", "Anesthesia", "Delirium" ], "interventions": [ { "name": "cerebral oximeter (Fore-Sight)", "type": "DEVICE" }, { "name": "depth of anesthesia monitor (BIS)", "type": "DEVICE" }, { "name": "BP management", "type": "PROCEDURE" }, { "name": "General anesthesia", "type": "PROCEDURE" }, { "name": "propofol", "type": "DRUG" }, { "name": "fentanyl", "type": "DRUG" }, { "name": "sevoflurane", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "PROCEDURE", "DRUG" ], "sponsor": "University of Missouri-Columbia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": null, "sex": "ALL", "summary": "65 Years and older" }, "enrollment_count": 145, "start_date": "2015-06-01", "completion_date": "2018-02-28", "has_results": true, "last_update_posted_date": "2023-10-17", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "Columbia, Missouri", "locations": [ { "city": "Columbia", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02604459" }, { "nct_id": "NCT06085586", "title": "Fibulink Syndesmosis Repair System With Early Full-Weight Bearing", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Ankle Fractures", "Bimalleolar Fractures", "Syndesmotic Injuries", "Bimalleolar Equivalent Fracture", "Maisonneuve Fracture", "Trimalleolar Fractures", "Ankle Dislocation" ], "interventions": [ { "name": "Early Weight Bearing", "type": "OTHER" }, { "name": "Normal Weight Bearing", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Maimonides Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "ALL", "summary": "22 Years and older" }, "enrollment_count": 56, "start_date": "2023-07-13", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-03-20", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "Brooklyn, New York", "locations": [ { "city": "Brooklyn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06085586" }, { "nct_id": "NCT03880188", "title": "Long Term Status of Free Dermal Fat Autografts for Complex Craniofacial Wounds", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Wounds and Injuries", "Wound Infection", "Facial Bones Fracture", "Soft Tissue Injuries", "Skull Fractures", "Surgical Wound", "Surgical Wound Infection", "Wound Healing", "Disturbance of Wound Healing", "Wound; Head, Multiple", "Wound; Head, Scalp", "Wound; Head", "Wound Complication", "Wound Dehiscence", "Wound of Skin", "Wound Open", "Wounds, Penetrating", "Wounds, Nonpenetrating", "Wounds" ], "interventions": [], "intervention_types": [], "sponsor": "Dufresne, Craig, MD, PC", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 20, "start_date": "2022-09-10", "completion_date": "2024-06-30", "has_results": false, "last_update_posted_date": "2022-06-16", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "Fairfax, Virginia", "locations": [ { "city": "Fairfax", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03880188" }, { "nct_id": "NCT00071032", "title": "Safety and Effectiveness of Two Blood Transfusion Strategies in Surgical Patients With Cardiovascular Disease", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Anemia", "Hematologic Diseases", "Cardiovascular Diseases", "Heart Diseases", "Myocardial Infarction", "Thromboembolism", "Pneumonia", "Cerebrovascular Accident" ], "interventions": [ { "name": "Liberal (10 g/dL) Transfusion Strategy", "type": "BIOLOGICAL" }, { "name": "Restrictive (Symptomatic) Transfusion Strategy", "type": "BIOLOGICAL" } ], "intervention_types": [ "BIOLOGICAL" ], "sponsor": "Rutgers, The State University of New Jersey", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 2016, "start_date": "2003-07", "completion_date": "2009-05", "has_results": true, "last_update_posted_date": "2020-11-16", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "New Brunswick, New Jersey", "locations": [ { "city": "New Brunswick", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT00071032" }, { "nct_id": "NCT01759407", "title": "Femoral Nerve Block for Femur Fracture Repair in Pediatrics", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Traumatic Femur Fracture" ], "interventions": [ { "name": "Ropivicaine", "type": "DRUG" }, { "name": "Epinephrine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Nationwide Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "18 Years", "sex": "ALL", "summary": "Up to 18 Years" }, "enrollment_count": 19, "start_date": "2013-05", "completion_date": "2016-10", "has_results": true, "last_update_posted_date": "2018-01-25", "last_synced_at": "2026-09-22T06:34:22.086Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01759407" } ] }