{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Pressure+Ulcers&page=2", "query": { "condition": "Pressure Ulcers", "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=Pressure+Ulcers&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-05-22T07:48:00.329Z", "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": "NCT01881815", "title": "Swab Sample Collection for the Detection of Bacterial Proteases", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Chronic Wounds" ], "interventions": [ { "name": "Swabs", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Systagenix Wound Management", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 141, "start_date": "2013-06", "completion_date": "2013-06", "has_results": false, "last_update_posted_date": "2013-07-08", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Tulsa, Oklahoma", "locations": [ { "city": "Tulsa", "state": "Oklahoma" } ], "official_url": "https://clinicaltrials.gov/study/NCT01881815" }, { "nct_id": "NCT02718625", "title": "Study of SANTYL® vs Hydrogel (SoloSite®) for Pressure Ulcers", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pressure Ulcer" ], "interventions": [ { "name": "Santyl", "type": "BIOLOGICAL" }, { "name": "SoloSite®", "type": "BIOLOGICAL" } ], "intervention_types": [ "BIOLOGICAL" ], "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": 3, "start_date": "2016-08", "completion_date": "2017-03-09", "has_results": true, "last_update_posted_date": "2020-03-10", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Lee's Summit, Missouri", "locations": [ { "city": "Lee's Summit", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02718625" }, { "nct_id": "NCT04884737", "title": "Decreasing Intraoperative Skin Damage in Prone Position Surgeries", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pressure Injury" ], "interventions": [ { "name": "Mepilex Border Flex® (MBF) dressing", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 107, "start_date": "2021-07-02", "completion_date": "2023-03-10", "has_results": true, "last_update_posted_date": "2023-05-31", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Santa Monica, California", "locations": [ { "city": "Santa Monica", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04884737" }, { "nct_id": "NCT03884634", "title": "Efficacy of the Dabir Surfaces Micropressure Overlay for Decubitus Ulcer Prevention During Cardiac Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Pressure Ulcer", "Pressure Injury" ], "interventions": [ { "name": "Dabir Micropressure Overlay", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6627, "start_date": "2019-03-01", "completion_date": "2022-09-15", "has_results": false, "last_update_posted_date": "2023-11-02", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03884634" }, { "nct_id": "NCT01433159", "title": "Comparison of HP011-101 to Standard Care for Stage I-II Pressure Ulcers in Subjects With Spinal Cord Injury", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Pressure Ulcers", "Spinal Cord Injury" ], "interventions": [ { "name": "HP011-101 (Xenaderm Ointment)", "type": "DRUG" }, { "name": "Standard Care", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Healthpoint", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": null, "sex": "ALL", "summary": "12 Years and older" }, "enrollment_count": 19, "start_date": "2011-09", "completion_date": "2013-01", "has_results": true, "last_update_posted_date": "2014-02-10", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 5, "location_summary": "Long Beach, California • San Jose, California • Tampa, Florida + 2 more", "locations": [ { "city": "Long Beach", "state": "California" }, { "city": "San Jose", "state": "California" }, { "city": "Tampa", "state": "Florida" }, { "city": "West Orange", "state": "New Jersey" }, { "city": "Charlotte", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01433159" }, { "nct_id": "NCT03450616", "title": "Pilot Study Comparing Negative Pressure Dressings to Conventional Dressings", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Venous Leg Ulcer" ], "interventions": [ { "name": "PICO Negative Pressure Wound Therapy", "type": "DEVICE" }, { "name": "Compression Dressing", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2019-06", "completion_date": "2019-12", "has_results": false, "last_update_posted_date": "2019-05-29", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Staten Island, New York", "locations": [ { "city": "Staten Island", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03450616" }, { "nct_id": "NCT01844479", "title": "Multi-layer Insoles for a Patient-specific Approach to Shear and Pressure Reduction in Diabetes-related Foot Ulcer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Foot Ulcer", "Diabetic Foot" ], "interventions": [ { "name": "diabetic foot orthotic", "type": "DEVICE" }, { "name": "Standard innersole", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "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": 27, "start_date": "2012-12", "completion_date": "2014-01", "has_results": true, "last_update_posted_date": "2016-10-06", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT01844479" }, { "nct_id": "NCT02375802", "title": "Adipose-Derived Stromal Cells (ASC's) for Pressure Ulcers", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Pressure Ulcer" ], "interventions": [ { "name": "Adipose-derived stromal cells", "type": "BIOLOGICAL" }, { "name": "Adipose-derived stromal cells", "type": "DRUG" } ], "intervention_types": [ "BIOLOGICAL", "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 12, "start_date": "2015-07", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-01-14", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02375802" }, { "nct_id": "NCT04776967", "title": "Effect of Total Compression Time and Rate (Slope) on Incidence of Symptomatic ETD and MEB: A Phase II Prospective Study.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Eustachian Tube Dysfunction", "Middle Ear Barotrauma", "Middle Ear Disease", "Middle Ear; Injury", "Pressure Injury", "Ear Barotrauma" ], "interventions": [ { "name": "Hyperbaric Compression Profile", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 300, "start_date": "2014-09-08", "completion_date": "2021-02-28", "has_results": false, "last_update_posted_date": "2021-08-19", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Sleepy Hollow, New York", "locations": [ { "city": "Sleepy Hollow", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04776967" }, { "nct_id": "NCT00262457", "title": "BIONs, for Improved Tissue Health and Pressure Sore Prevention", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pressure Ulcers", "Spinal Cord Injury" ], "interventions": [ { "name": "Implanted gluteal electrical stimulation system", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "US Department of Veterans Affairs", "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": 0, "start_date": "2004-04", "completion_date": "2008-02", "has_results": false, "last_update_posted_date": "2013-09-17", "last_synced_at": "2026-05-22T07:48:00.329Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT00262457" } ] }