{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Complications+Wounds&page=17", "query": { "condition": "Complications Wounds", "page": 17 }, "page_size": 10 }, "pagination": { "page": 17, "page_size": 10, "total_count": 447, "total_pages": 45, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Complications+Wounds&page=18&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Complications+Wounds&page=16&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-24T06:02:12.246Z", "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": "NCT02742974", "title": "Fluid Resuscitation Optimization in Surgical Trauma Patients (FROST)", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Critical Illness", "Trauma" ], "interventions": [ { "name": "Device: FloTrac™ and EV1000™", "type": "DEVICE" }, { "name": "Volume Challenge", "type": "OTHER" }, { "name": "Vasopressor Therapy", "type": "DRUG" }, { "name": "Inotropic Therapy", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "OTHER", "DRUG" ], "sponsor": "CAMC Health System", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 48, "start_date": "2015-10", "completion_date": "2017-11", "has_results": false, "last_update_posted_date": "2026-09-09", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 1, "location_summary": "Charleston, West Virginia", "locations": [ { "city": "Charleston", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02742974" }, { "nct_id": "NCT05383417", "title": "No Post Intubation Laryngeal Symptoms", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sore-throat", "Dysphonia", "Dysphagia", "Intubation Complication", "Anesthesia Intubation Complication", "Anesthesia Morbidity", "Anesthesia Complication", "Anesthesia; Adverse Effect", "Anesthesia; Reaction", "Throat Disorder", "Throat; Wound", "Throat Injury" ], "interventions": [ { "name": "EndoClip", "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": 100, "start_date": "2022-11-08", "completion_date": "2023-09-21", "has_results": true, "last_update_posted_date": "2025-09-10", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05383417" }, { "nct_id": "NCT02436876", "title": "Study to Assess Safety and Clinical Activity of Local MBN-101 in Treatment of Infected Bone Sites", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Bacterial Infection" ], "interventions": [ { "name": "MBN-101", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Microbion Corporation", "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": 29, "start_date": "2016-05-24", "completion_date": "2018-07-26", "has_results": true, "last_update_posted_date": "2021-09-30", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 6, "location_summary": "San Francisco, California • Baltimore, Maryland • Columbus, Ohio + 2 more", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "Columbus", "state": "Ohio" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02436876" }, { "nct_id": "NCT00457600", "title": "ParentLink: Better and Safer Emergency Care for Children", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Otitis Media", "Urinary Tract Infection", "Asthma", "Head Injury" ], "interventions": [ { "name": "patient-driven health IT product", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Boston Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "12 Years", "sex": "ALL", "summary": "Up to 12 Years" }, "enrollment_count": 3000, "start_date": "2005-06", "completion_date": "2006-07", "has_results": false, "last_update_posted_date": "2007-04-06", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 2, "location_summary": "Boston, Massachusetts • Weymouth, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Weymouth", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00457600" }, { "nct_id": "NCT03284983", "title": "Split Scar Study to Assess Cosmetic Outcome From Differing Suture Spacing", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suture, Complication", "Wound", "Wound Complication", "Wound Dehiscence", "Wound of Skin", "Surgery", "Suture; Complications, Infection or Inflammation" ], "interventions": [ { "name": "Suture spacing for wound closure", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Silver Falls Dermatology", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "30 Years to 100 Years" }, "enrollment_count": 30, "start_date": "2017-07-01", "completion_date": "2017-10-01", "has_results": false, "last_update_posted_date": "2017-09-15", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 1, "location_summary": "Salem, Oregon", "locations": [ { "city": "Salem", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT03284983" }, { "nct_id": "NCT01601223", "title": "Local Assessment of Ventilatory Management During General Anesthesia for Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Surgery", "Anaesthesia", "Ventilator-Induced Lung Injury", "Lung Injury", "Pneumonia", "Pneumothorax", "Respiratory Distress Syndrome, Adult", "Respiratory Insufficiency" ], "interventions": [], "intervention_types": [], "sponsor": "European Society of Anaesthesiology", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 10690, "start_date": "2013-01", "completion_date": "2013-11", "has_results": false, "last_update_posted_date": "2015-10-14", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 3, "location_summary": "Aurora, Colorado • Boston, Massachusetts • Rochester, Minnesota", "locations": [ { "city": "Aurora", "state": "Colorado" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT01601223" }, { "nct_id": "NCT05231460", "title": "Pain Management Study", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pain, Postoperative" ], "interventions": [ { "name": "Active Comparator: narcotic regimen with TAP block", "type": "DRUG" }, { "name": "Active Comparator: narcotic regimen with no TAP block", "type": "DRUG" }, { "name": "non-narcotic regimen with TAP block", "type": "DRUG" }, { "name": "non-narcotic regimen with no TAP block", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Arizona", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 244, "start_date": "2022-02-18", "completion_date": "2026-06", "has_results": false, "last_update_posted_date": "2025-08-24", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 1, "location_summary": "Phoenix, Arizona", "locations": [ { "city": "Phoenix", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT05231460" }, { "nct_id": "NCT00880295", "title": "Patient Outcomes With Endoscopic Versus Open Carpal Tunnel Release", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Carpal Tunnel Syndrome" ], "interventions": [ { "name": "endoscopic carpal tunnel release", "type": "PROCEDURE" }, { "name": "open carpal tunnel release", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Penn State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 38, "start_date": "2009-03-23", "completion_date": "2016-07-26", "has_results": false, "last_update_posted_date": "2017-11-24", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 1, "location_summary": "Hershey, Pennsylvania", "locations": [ { "city": "Hershey", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00880295" }, { "nct_id": "NCT06559137", "title": "Evaluation of Pain Management After Surgery When Using Nerve Blocks in the Pediatric Population", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Anterior Cruciate Ligament (ACL) Tear", "Sports Injuries in Children", "Analgesia", "Pain, Postoperative" ], "interventions": [ { "name": "Ropivacaine 0.2% Injectable Solution", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Texas Scottish Rite Hospital for Children", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "13 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "13 Years to 21 Years" }, "enrollment_count": 160, "start_date": "2025-09", "completion_date": "2028-09", "has_results": false, "last_update_posted_date": "2025-09-16", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 1, "location_summary": "Frisco, Texas", "locations": [ { "city": "Frisco", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06559137" }, { "nct_id": "NCT00458471", "title": "E. Coli for Prevention of Catheter UTI in SCI Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Urinary Tract Infection(UTI)" ], "interventions": [ { "name": "Insertion of a urinary catheter coated with benign E. coli", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 12, "start_date": "2003-11", "completion_date": "2005-07", "has_results": false, "last_update_posted_date": "2007-04-10", "last_synced_at": "2026-10-24T06:02:12.246Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00458471" } ] }