{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Injury+Foot&page=4", "query": { "condition": "Injury Foot", "page": 4 }, "page_size": 10 }, "pagination": { "page": 4, "page_size": 10, "total_count": 283, "total_pages": 29, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Injury+Foot&page=5&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Injury+Foot&page=3&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-20T10:00:11.850Z", "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": "NCT07052721", "title": "Randomized Study of an Analgesic Device Enabling Local Anesthetic Delivery and Neuromodulation After Shoulder/Foot Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Rotator Cuff Tears", "Shoulder Injuries", "Hallux Valgus", "Ankle Arthropathy", "Clavicle Fracture" ], "interventions": [ { "name": "Experimental Treatment", "type": "DEVICE" }, { "name": "Sham Comparator", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 44, "start_date": "2025-09-05", "completion_date": "2026-06-26", "has_results": false, "last_update_posted_date": "2026-07-27", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07052721" }, { "nct_id": "NCT03321721", "title": "Cosmetic Outcome at 4 Months in Hand and Feet Lacerations in Children: Conservative Versus Suture Repair", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Laceration Repair, Children", "Hand Injuries", "Foot Injuries" ], "interventions": [ { "name": "Suture for wound repair", "type": "PROCEDURE" }, { "name": "Suture for wound repair", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DEVICE" ], "sponsor": "St. Louis University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "2 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "2 Years to 17 Years" }, "enrollment_count": 26, "start_date": "2014-04-13", "completion_date": "2019-05", "has_results": true, "last_update_posted_date": "2020-10-09", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03321721" }, { "nct_id": "NCT02280733", "title": "A Real-World Registry of Chronic Wounds and Ulcers", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diabetic Foot", "Pressure Ulcer", "Surgical Wound Dehiscence", "Vasculitis", "Skin Ulcer", "Leg Ulcer", "Pyoderma", "Peripheral Arterial Disease", "Lymphedema", "Surgical Complication", "Venous Leg Ulcers (VLUs)", "Calciphylaxis", "Sickle Cell Ulcer", "Pressure Ulcer (PU)", "Diabetic Foot Ulcers (DFUs)", "Pressure Injury", "Arterial Ulcers", "Soft Tissue Radionecrosis (STRN)", "Traumatic Wounds", "Chronic Ulcer" ], "interventions": [ { "name": "Usual care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "U.S. Wound Registry", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 300000, "start_date": "2005-01-01", "completion_date": "2030-01", "has_results": false, "last_update_posted_date": "2025-07-16", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 1, "location_summary": "The Woodlands, Texas", "locations": [ { "city": "The Woodlands", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02280733" }, { "nct_id": "NCT07852338", "title": "a Prospective, Multicenter, Randomized Controlled Trial, With a Non-randomized Sentinel Cohort, Evaluating the Efficacy of Bioxheal, a Single-layer Placental-derived Biologic in Nonhealing Diabetic Foot Ulcers", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Diabetic Foot Ulcer", "Amniotic Membrane Placental Allograft", "Biologic" ], "interventions": [ { "name": "Standard of Care", "type": "OTHER" }, { "name": "BIOxHEAL (human amniotic membrane allograft)", "type": "BIOLOGICAL" } ], "intervention_types": [ "OTHER", "BIOLOGICAL" ], "sponsor": "Applied Biologics, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 253, "start_date": "2026-10-08", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2026-10-16", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 1, "location_summary": "Boardman, Ohio", "locations": [ { "city": "Boardman", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07852338" }, { "nct_id": "NCT06384183", "title": "Kerecis Real-World Fish Skin Graft Registry", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Wounds", "Pressure Ulcer", "Diabetic Foot Ulcer", "Venous Leg Ulcer", "Surgical Wound", "Soft Tissue Reinforcement" ], "interventions": [ { "name": "Kerecis Fish Skin Graft", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Kerecis Ltd.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 600, "start_date": "2024-08-07", "completion_date": "2027-06", "has_results": false, "last_update_posted_date": "2024-12-30", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 6, "location_summary": "Sarasota, Florida • Greensboro, North Carolina • Beavercreek, Ohio + 2 more", "locations": [ { "city": "Sarasota", "state": "Florida" }, { "city": "Sarasota", "state": "Florida" }, { "city": "Greensboro", "state": "North Carolina" }, { "city": "Beavercreek", "state": "Ohio" }, { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT06384183" }, { "nct_id": "NCT01816672", "title": "Efficacy of AutoloGel Therapy to Usual and Customary Care in Wagner gd 1 and 2 Diabetic Foot Ulcers.", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Foot Ulcer" ], "interventions": [ { "name": "AutoloGel", "type": "DEVICE" }, { "name": "Usual and Customary Care", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Cytomedix", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 4, "start_date": "2013-04", "completion_date": "2015-07", "has_results": false, "last_update_posted_date": "2016-10-21", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 1, "location_summary": "Hattiesburg, Mississippi", "locations": [ { "city": "Hattiesburg", "state": "Mississippi" } ], "official_url": "https://clinicaltrials.gov/study/NCT01816672" }, { "nct_id": "NCT02294175", "title": "Larval Debridement Therapy Versus Sharp Debridement to Remove Biofilm", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lower Extremity or Diabetic Foot Ulcers", "Bacterial Infection" ], "interventions": [ { "name": "Larval Debridement Therapy", "type": "DEVICE" }, { "name": "Bedside Sharp Debridement", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "North Florida Foundation for Research and Education", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 45, "start_date": "2015-01", "completion_date": "2018-03-24", "has_results": true, "last_update_posted_date": "2020-04-07", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 2, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02294175" }, { "nct_id": "NCT00761176", "title": "A Pilot Study of the Provant Therapy System in Subjects With Diabetic Foot Ulcers", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Foot Ulcers" ], "interventions": [ { "name": "The Provant Therapy System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Regenesis Biomedical, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 8, "start_date": "2008-07", "completion_date": "2011-03", "has_results": true, "last_update_posted_date": "2016-01-05", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00761176" }, { "nct_id": "NCT04182451", "title": "Effect of Meso Wound Matrix in the Treatment of DFUs", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Foot Ulcers (DFUs)" ], "interventions": [ { "name": "Meso Wound Matrix", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "SerenaGroup, Inc.", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2019-12-05", "completion_date": "2023-03-01", "has_results": false, "last_update_posted_date": "2023-04-26", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 3, "location_summary": "Pembroke Pines, Florida • Ford City, Pennsylvania • Pittsburgh, Pennsylvania", "locations": [ { "city": "Pembroke Pines", "state": "Florida" }, { "city": "Ford City", "state": "Pennsylvania" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04182451" }, { "nct_id": "NCT07287969", "title": "The Safety of Reusing Walking Boot Components for Patients Recovering From Acute Foot and Ankle Injuries", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Foot Injuries", "Ankle Injuries" ], "interventions": [ { "name": "New durable medical equipment (DME) walking boot", "type": "DEVICE" }, { "name": "Re-used durable medical equipment (DME) walking boot", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": "17 Years", "sex": "ALL", "summary": "1 Year to 17 Years" }, "enrollment_count": 60, "start_date": "2024-09-25", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2026-08-13", "last_synced_at": "2026-10-20T10:00:11.850Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT07287969" } ] }