{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Skin+Patch&page=13", "query": { "intervention": "Skin Patch", "page": 13 }, "page_size": 10 }, "pagination": { "page": 13, "page_size": 10, "total_count": 1598, "total_pages": 160, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Skin+Patch&page=14&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Skin+Patch&page=12&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-02T04:38:27.895Z", "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": "NCT05741476", "title": "Safety and Efficacy Study of Viaskin Peanut in Peanut-allergic Children 4-7 Years of Age", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Allergy, Peanut" ], "interventions": [ { "name": "DBV712", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "DBV Technologies", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "4 Years", "maximum_age": "7 Years", "sex": "ALL", "summary": "4 Years to 7 Years" }, "enrollment_count": 600, "start_date": "2023-02-21", "completion_date": "2029-10", "has_results": false, "last_update_posted_date": "2026-01-22", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 50, "location_summary": "Birmingham, Alabama • Tucson, Arizona • Little Rock, Arkansas + 42 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05741476" }, { "nct_id": "NCT03982511", "title": "Improving Parent-Child Interactions to Enhance Child Health", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Child Obesity" ], "interventions": [ { "name": "PCIT-Health", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Central Michigan University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Months", "maximum_age": "84 Months", "sex": "ALL", "summary": "30 Months to 84 Months" }, "enrollment_count": 63, "start_date": "2019-05-29", "completion_date": "2022-04-08", "has_results": true, "last_update_posted_date": "2023-09-15", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 1, "location_summary": "Mount Pleasant, Michigan", "locations": [ { "city": "Mount Pleasant", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03982511" }, { "nct_id": "NCT00403234", "title": "Safety of Buprenorphine Transdermal System (BTDS) in Subjects With Acute Postoperative Pain After Total Knee Replacement", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "Buprenorphine transdermal patch", "type": "DRUG" }, { "name": "Placebo BTDS", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Purdue Pharma LP", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 10, "start_date": "2006-11", "completion_date": "2007-08", "has_results": true, "last_update_posted_date": "2012-09-03", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 5, "location_summary": "Phoenix, Arizona • San Clemente, California • Orlando, Florida + 2 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "San Clemente", "state": "California" }, { "city": "Orlando", "state": "Florida" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "Sewickley", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00403234" }, { "nct_id": "NCT00532116", "title": "PK Comparison of 6mg and 12mg EMSAM in Elderly vs. Non-Elderly", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Healthy" ], "interventions": [ { "name": "EMSAM (Selegiline Transdermal System) 6mg", "type": "DRUG" }, { "name": "EMSAM (Selegiline Transdermal System) 12mg", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Somerset Pharmaceuticals", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 32, "start_date": "2007-04", "completion_date": "2007-08", "has_results": false, "last_update_posted_date": "2007-09-19", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 1, "location_summary": "Honolulu, Hawaii", "locations": [ { "city": "Honolulu", "state": "Hawaii" } ], "official_url": "https://clinicaltrials.gov/study/NCT00532116" }, { "nct_id": "NCT00775749", "title": "Transdermal Nicotine in Female Patients at High Risk for Post Operative Nausea and/or Vomiting (PONV)", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Nausea and Vomiting" ], "interventions": [ { "name": "transdermal nicotine patch", "type": "DRUG" }, { "name": "placebo patch", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Ochsner Health System", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 0, "start_date": "2009-04", "completion_date": "2012-04", "has_results": false, "last_update_posted_date": "2023-04-11", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 1, "location_summary": "New Orleans, Louisiana", "locations": [ { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT00775749" }, { "nct_id": "NCT00223717", "title": "Treatment of Supine Hypertension in Autonomic Failure", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Hypertension" ], "interventions": [ { "name": "Clonidine", "type": "DRUG" }, { "name": "Nitroglycerin transdermal", "type": "DRUG" }, { "name": "Dipyridamole/ Aspirin (Aggrenox)", "type": "DRUG" }, { "name": "Desmopressin (DDAVP)", "type": "DRUG" }, { "name": "Sildenafil", "type": "DRUG" }, { "name": "Nifedipine", "type": "DRUG" }, { "name": "Hydralazine", "type": "DRUG" }, { "name": "Hydrochlorothiazide", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Bosentan", "type": "DRUG" }, { "name": "Diltiazem", "type": "DRUG" }, { "name": "Eplerenone", "type": "DRUG" }, { "name": "guanfacine", "type": "DRUG" }, { "name": "L-arginine", "type": "DIETARY_SUPPLEMENT" }, { "name": "captopril", "type": "DRUG" }, { "name": "carbidopa", "type": "DRUG" }, { "name": "losartan", "type": "DRUG" }, { "name": "metoprolol tartrate", "type": "DRUG" }, { "name": "nebivolol hydrochloride", "type": "DRUG" }, { "name": "prazosin hydrochloride", "type": "DRUG" }, { "name": "tamsulosin hydrochloride", "type": "DRUG" }, { "name": "Head-up tilt.", "type": "OTHER" }, { "name": "aliskiren", "type": "DRUG" }, { "name": "Local heat stress", "type": "OTHER" } ], "intervention_types": [ "DRUG", "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Vanderbilt University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 152, "start_date": "2001-01", "completion_date": "2017-01", "has_results": false, "last_update_posted_date": "2017-10-13", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT00223717" }, { "nct_id": "NCT02358135", "title": "Collaborative Connected Health (CCH) for PCORI", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Psoriasis" ], "interventions": [ { "name": "Collaborative Connected health, (CCH)", "type": "OTHER" }, { "name": "Control", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Southern California", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2015-02-02", "completion_date": "2017-08-20", "has_results": true, "last_update_posted_date": "2019-08-28", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 3, "location_summary": "Los Angeles, California • Sacramento, California • Aurora, Colorado", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Sacramento", "state": "California" }, { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT02358135" }, { "nct_id": "NCT06042140", "title": "Cryopreserved Human Umbilical Cord as a Meningeal Patch in Fetoscopic Spina Bifida Repair", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spina Bifida; Fetus", "Myelomeningocele", "Myeloschisis" ], "interventions": [ { "name": "NEOX Cord 1K applied fetoscopically", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 100, "start_date": "2023-09-08", "completion_date": "2036-09-08", "has_results": false, "last_update_posted_date": "2025-08-13", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06042140" }, { "nct_id": "NCT04796935", "title": "A Study to Test Performance of Needle Placements for Neuraxial Procedures Using Tactile Imaging vs Control", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Central Nervous System Infections", "Pseudotumor Cerebri", "Neurological Disorder", "Cancer", "Obstetric Procedure Pain", "Orthopedic Procedure Pain", "Post-Dural Puncture Headache" ], "interventions": [ { "name": "Tactile Imaging (VerTouch)", "type": "DEVICE" }, { "name": "Control (palpation)", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "IntuiTap Medical, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 95, "start_date": "2021-04-04", "completion_date": "2021-11-24", "has_results": true, "last_update_posted_date": "2024-06-11", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 3, "location_summary": "Providence, Rhode Island • Charleston, South Carolina • Houston, Texas", "locations": [ { "city": "Providence", "state": "Rhode Island" }, { "city": "Charleston", "state": "South Carolina" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04796935" }, { "nct_id": "NCT00664755", "title": "Menstrual Cycle Effects on Smoking Cessation and Cue Reactivity", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Nicotine Dependence" ], "interventions": [ { "name": "varenicline", "type": "DRUG" }, { "name": "transdermal nicotine patch", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 140, "start_date": "2007-07", "completion_date": "2013-12", "has_results": true, "last_update_posted_date": "2018-05-24", "last_synced_at": "2026-11-02T04:38:27.895Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00664755" } ] }