{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=lidocaine+hydrochloride", "query": { "intervention": "lidocaine hydrochloride" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 965, "total_pages": 97, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=lidocaine+hydrochloride&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-30T21:30:13.348Z", "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": "NCT04537026", "title": "Sterile Amniotic Fluid Filtrate Epidural Injection.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Lumbar Spinal Stenosis" ], "interventions": [ { "name": "Amniotic Fluid Allograft", "type": "DRUG" }, { "name": "Dexamethasone sodium phosphate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 58, "start_date": "2021-06-16", "completion_date": "2025-07-01", "has_results": true, "last_update_posted_date": "2026-09-25", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT04537026" }, { "nct_id": "NCT03676725", "title": "Prevalence of Lidocaine Ineffectiveness in Adults With and Without ADHD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "ADHD", "PMS" ], "interventions": [ { "name": "Lidocaine gel", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "PhenoSolve, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "49 Years", "sex": "ALL", "summary": "18 Years to 49 Years" }, "enrollment_count": 90, "start_date": "2019-08-14", "completion_date": "2020-03-01", "has_results": true, "last_update_posted_date": "2022-10-06", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 2, "location_summary": "Boston, Massachusetts • The Bronx, New York", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03676725" }, { "nct_id": "NCT00110734", "title": "S-Caine™ Peel (Skin Numbing Cream) to Treat Pain During Laser-Assisted Tattoo Removal in Adults", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Pain" ], "interventions": [ { "name": "S-Caine™ Peel (lidocaine and tetracaine cream 7%/7%)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "ZARS Pharma Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": null, "completion_date": "2005-09", "has_results": false, "last_update_posted_date": "2005-09-23", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00110734" }, { "nct_id": "NCT03301766", "title": "Adjunctive 5% Lidocaine Patches for Acute Non-radicular Low Back Pain in Emergency Department Patients", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Low Back Pain" ], "interventions": [ { "name": "lidocaine 5% patch", "type": "DRUG" }, { "name": "standard therapy", "type": "DRUG" }, { "name": "Non-medicated patch", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Cook County Health", "sponsor_class": "OTHER_GOV", "healthy_volunteers": false, "eligibility": { "minimum_age": "24 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "24 Years to 64 Years" }, "enrollment_count": 0, "start_date": "2017-03-10", "completion_date": "2023-05-22", "has_results": false, "last_update_posted_date": "2023-06-29", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03301766" }, { "nct_id": "NCT05589402", "title": "Temporary Inactivation of Strong Muscle Sensation to Improve Rehabilitation Interventions in SCI", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Spinal Cord Injuries", "Spine Disease", "Stroke" ], "interventions": [ { "name": "Lidocaine Cream 5%", "type": "DRUG" }, { "name": "Rehabilitation Movement Training", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of Texas Rio Grande Valley", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 52, "start_date": "2019-06-04", "completion_date": "2026-07-15", "has_results": false, "last_update_posted_date": "2026-07-31", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "Harlingen, Texas", "locations": [ { "city": "Harlingen", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05589402" }, { "nct_id": "NCT06514430", "title": "Prophylactic Analgesia for Bladder Botox Injections", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Urinary Incontinence", "Urinary Incontinence, Urge", "Overactive Bladder" ], "interventions": [ { "name": "Phenazopyridine", "type": "DRUG" }, { "name": "1% lidocaine with sodium bicarbonate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Montefiore Medical Center", "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": 0, "start_date": "2025-07", "completion_date": "2026-02", "has_results": false, "last_update_posted_date": "2025-07-18", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "The Bronx, New York", "locations": [ { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06514430" }, { "nct_id": "NCT04760483", "title": "Office Based Transperineal Laser Ablation for Benign Prostatic Hyperplasia HYPERPLASIA", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Male Urogenital Diseases", "Genital Diseases, Male", "Prostatic Disease", "Prostatic Hyperplasia" ], "interventions": [ { "name": "SoracteLite(TM) TPLA for BPH", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Urological Research Network, LLC", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": "85 Years", "sex": "MALE", "summary": "40 Years to 85 Years · Male only" }, "enrollment_count": 20, "start_date": "2020-11-20", "completion_date": "2026-03-20", "has_results": false, "last_update_posted_date": "2023-01-26", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "Hialeah, Florida", "locations": [ { "city": "Hialeah", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04760483" }, { "nct_id": "NCT03046017", "title": "Neuromodulation of Lidocaine Cream Effect on Chronic Pain Patients", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Low Back Pain" ], "interventions": [ { "name": "tDCS", "type": "DEVICE" }, { "name": "Lidocaine cream", "type": "OTHER" }, { "name": "Control cream", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "21 Years to 60 Years" }, "enrollment_count": 90, "start_date": "2017-08-30", "completion_date": "2023-05", "has_results": false, "last_update_posted_date": "2023-01-03", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "Charlestown, Massachusetts", "locations": [ { "city": "Charlestown", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03046017" }, { "nct_id": "NCT00656110", "title": "Neuroma Injections to Treat Restless Legs Syndrome - RCT", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Restless Legs Syndrome" ], "interventions": [ { "name": "equal parts of 0.5% plain Marcaine and 2% lidocaine mixed with 0.8 mg Depo-medrol/4% absolute alcohol in a total injection volume of 1 ml", "type": "DRUG" }, { "name": "Normal saline - 1ml", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Lowcountry Infectious Diseases", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2008-04", "completion_date": "2009-12", "has_results": false, "last_update_posted_date": "2009-03-10", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00656110" }, { "nct_id": "NCT03936309", "title": "A Comparison of Scar Infiltration, Scar Deactivation, and Standard of Care for the Treatment of Chronic, Post-Surgical Pain After Cesarean Section", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Scar", "Cesarean Section; Dehiscence" ], "interventions": [ { "name": "Scar Deactivation Surface Release Technique protocol", "type": "OTHER" }, { "name": "Scar Infiltration with 0.25-1% Lidocaine", "type": "OTHER" }, { "name": "Physical therapy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Jennifer Loomis", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 60, "start_date": "2019-06-01", "completion_date": "2025-04-08", "has_results": false, "last_update_posted_date": "2025-04-09", "last_synced_at": "2026-09-30T21:30:13.348Z", "location_count": 1, "location_summary": "Scott Air Force Base, Illinois", "locations": [ { "city": "Scott Air Force Base", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03936309" } ] }