{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Complications+Wounds&page=15", "query": { "condition": "Complications Wounds", "page": 15 }, "page_size": 10 }, "pagination": { "page": 15, "page_size": 10, "total_count": 447, "total_pages": 45, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Complications+Wounds&page=16&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Complications+Wounds&page=14&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T16:13:22.387Z", "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": "NCT00942890", "title": "Strength, Pain and Function in Operation Iraqi Freedom/Operation Enduring Freedom Amputees: A Nurse-Managed Program", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Traumatic Amputation" ], "interventions": [ { "name": "NMES (EMPI 300PV stimulator) plus standard of care", "type": "DEVICE" }, { "name": "TMARP standard of care", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "University of Tennessee", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 44, "start_date": "2009-04", "completion_date": "2015-08", "has_results": true, "last_update_posted_date": "2018-04-10", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 3, "location_summary": "San Diego, California • Bethesda, Maryland • Memphis, Tennessee", "locations": [ { "city": "San Diego", "state": "California" }, { "city": "Bethesda", "state": "Maryland" }, { "city": "Memphis", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT00942890" }, { "nct_id": "NCT06949826", "title": "Buprenorphine as a Post-operative Analgesic in Opioid-Naive Patients After Ankle Fracture Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pain, Postoperative", "Ankle Fracture Surgery", "Opioid Use Disorder", "Opioid Dependence", "Opioid Analgesia" ], "interventions": [ { "name": "Buprenorphine Transdermal System", "type": "DRUG" }, { "name": "Placebo Patch", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Jenna-Leigh Wilson", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2025-04-21", "completion_date": "2027-06", "has_results": false, "last_update_posted_date": "2026-04-06", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT06949826" }, { "nct_id": "NCT04806620", "title": "Unhide® Project: A Digital Health Platform to Collect Lifestyle Data for Brain Inflammation Research", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Post-Acute COVID-19 Syndrome", "ME/CFS", "Rheumatic Arthritis", "Juvenile Rheumatoid Arthritis (JRA)", "Psoriatic Arthritis (PsA)", "Ankylosing Spondylitis (AS)", "Autoimmune Encephalitis", "Celiac Disease", "Celiac Disease in Children", "Chronic Lyme Disease", "Post-treatment Lyme Disease Syndrome", "Crohn's Disease", "Dysautonomia", "Anorexia Nervosa", "Bulimia Nervosa", "ARFID", "Avoidant / Restrictive Food Intake Disorder", "Ehlers Danlos Syndrome", "Endometriosis", "Fibromyalgia (FM)", "Long COVID", "Lupus", "Migraines", "Mast Cell Activation Syndrome", "Multiple Sclerosis", "Myalgic Encephalomyelitis (ME)", "Myasthenia Gravis, Generalized", "Myasthenia Gravis in Children", "Narcolepsy", "Obsessive Compulsive Disorder (OCD)", "PANDAS", "Pediatric Acute-onset Neuropsychiatric Syndrome (PANS)", "POTS - Postural Orthostatic Tachycardia Syndrome", "General Anxiety Disorder, Social Anxiety Disorder", "PTSD - Post Traumatic Stress Disorder", "Psoriasis", "Traumatic Brain Injury", "Tourette's Syndrome", "Inflammatory Bowel Disease (IBD)", "Autoimmune Diseases", "Neurological Diseases or Conditions", "Psychiatric Disorder", "Sjogren's Syndrome", "Ulcerative Colitis and Crohn's Disease" ], "interventions": [], "intervention_types": [], "sponsor": "Brain Inflammation Collaborative", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 10000, "start_date": "2023-07-05", "completion_date": "2030-12-31", "has_results": false, "last_update_posted_date": "2026-01-22", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 1, "location_summary": "Delafield, Wisconsin", "locations": [ { "city": "Delafield", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT04806620" }, { "nct_id": "NCT04210609", "title": "Effectiveness of Vaporous Hyperoxia Therapy (VHT) in the Treatment of Chronic Diabetic Foot Ulcers", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Foot Ulcer" ], "interventions": [ { "name": "Vaporous Hyperoxia Therapy", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Vaporox", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 30, "start_date": "2021-10-04", "completion_date": "2022-10-03", "has_results": false, "last_update_posted_date": "2021-10-11", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 3, "location_summary": "Castle Rock, Colorado • Denver, Colorado", "locations": [ { "city": "Castle Rock", "state": "Colorado" }, { "city": "Denver", "state": "Colorado" }, { "city": "Denver", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04210609" }, { "nct_id": "NCT05090800", "title": "Contrast Enhanced Ultrasound for Renal Obstruction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Kidney; Obstruction", "Renal Obstruction" ], "interventions": [ { "name": "Definity contrast during ultrasound", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 10, "start_date": "2021-12-03", "completion_date": "2025-09-23", "has_results": false, "last_update_posted_date": "2025-10-02", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05090800" }, { "nct_id": "NCT06189781", "title": "Pain Injection Versus Epidural Anesthesia for Hip Surgery in Pediatric Patients With Cerebral Palsy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cerebral Palsy", "Hip Dysplasia", "Pain, Postoperative" ], "interventions": [ { "name": "Ropivacaine injection", "type": "DRUG" }, { "name": "Bupivacaine, lidocaine, ropivacaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "18 Years", "sex": "ALL", "summary": "Up to 18 Years" }, "enrollment_count": 90, "start_date": "2023-12-01", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2024-06-11", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 4, "location_summary": "Los Angeles, California • Santa Monica, California • Chicago, Illinois", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Santa Monica", "state": "California" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06189781" }, { "nct_id": "NCT03026647", "title": "Suture Material for Closure of Hysterotomy", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cesarean Section; Complications, Wound, Hematoma" ], "interventions": [ { "name": "Suture", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "St. Louis University", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "14 Years", "maximum_age": "55 Years", "sex": "FEMALE", "summary": "14 Years to 55 Years · Female only" }, "enrollment_count": 0, "start_date": "2017-01-31", "completion_date": "2018-05", "has_results": false, "last_update_posted_date": "2017-11-13", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03026647" }, { "nct_id": "NCT03967847", "title": "Oral Ketorolac for Arthroscopic Rotator Cuff Repair", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Rotator Cuff Tear", "Postoperative Pain" ], "interventions": [ { "name": "Ketorolac", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University Hospitals Cleveland Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 44, "start_date": "2019-02-11", "completion_date": "2021-05-17", "has_results": true, "last_update_posted_date": "2022-05-10", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03967847" }, { "nct_id": "NCT00662207", "title": "Two Devices for Reflex Voiding Following Spinal Cord Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Spinal Cord Injury", "Urinary Incontinence" ], "interventions": [ { "name": "Vibrator", "type": "DEVICE" }, { "name": "Anal dilator", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "US Department of Veterans Affairs", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "MALE", "summary": "18 Years to 70 Years · Male only" }, "enrollment_count": 3, "start_date": "2008-10", "completion_date": "2009-10", "has_results": true, "last_update_posted_date": "2014-11-05", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 1, "location_summary": "Hines, Illinois", "locations": [ { "city": "Hines", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00662207" }, { "nct_id": "NCT05783245", "title": "Effect of Cooling Therapy for Post-Operative Pain in Open Carpal Tunnel Release", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Carpal Tunnel Syndrome", "Perioperative/Postoperative Complications" ], "interventions": [ { "name": "Polarcare Machine", "type": "OTHER" }, { "name": "Standard of care ice therapy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 128, "start_date": "2023-06-01", "completion_date": "2026-09-30", "has_results": false, "last_update_posted_date": "2026-02-05", "last_synced_at": "2026-10-23T16:13:22.387Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05783245" } ] }