{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Non-Invasive+Treatment&page=2", "query": { "intervention": "Non-Invasive Treatment", "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?intervention=Non-Invasive+Treatment&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-09T18:23:50.978Z", "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": "NCT03772873", "title": "MIPE for Pilonidal Disease", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Pilonidal Disease", "Pilonidal Cyst/Fistula", "Pilonidal Sinus Without Abscess", "Pilonidal Cyst Without Abscess", "Pilonidal Cyst and Sinus Without Abscess", "Pilonidal Abscess", "Pilonidal Sinus With Abscess", "Pilonidal Dimple With Abscess", "Pilonidal Fistula With Abscess", "Pilonidal Sinus Infected", "Pilonidal Cyst With Sinus", "Pilonidal Cyst and Sinus With Abscess", "Pilonidal Disease of Natal Cleft Abscess" ], "interventions": [ { "name": "minimally invasive pilonidal excision", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "2 Years to 25 Years" }, "enrollment_count": 151, "start_date": "2019-01-01", "completion_date": "2026-06-01", "has_results": false, "last_update_posted_date": "2022-11-17", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 10, "location_summary": "Chicago, Illinois • Park Ridge, Illinois • Portland, Maine + 7 more", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Park Ridge", "state": "Illinois" }, { "city": "Portland", "state": "Maine" }, { "city": "Baltimore", "state": "Maryland" }, { "city": "New Hyde Park", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03772873" }, { "nct_id": "NCT00486512", "title": "Chemoprevention of Colorectal Adenomas", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Adenomatous Polyps" ], "interventions": [ { "name": "0.5 mg calcitriol (1a -25-dihydroxycholecalciferol)", "type": "DRUG" }, { "name": "75 mg acetylsalicylic acid (ASA) + 1250 mg calcium carbonate (CaCO3)", "type": "DRUG" }, { "name": "placebo to 0.5 mg calcitriol (1a -25-dihydroxycholecalciferol)", "type": "DRUG" }, { "name": "placebo to 75 mg acetylsalicylic acid (ASA) + 1250 mg calcium carbonate (CaCO3)", "type": "DRUG" }, { "name": "Colonoscopy", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "Colotech A/S", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "40 Years to 75 Years" }, "enrollment_count": 350, "start_date": "2007-06", "completion_date": "2010-11", "has_results": false, "last_update_posted_date": "2020-09-03", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 24, "location_summary": "Huntsville, Alabama • San Diego, California • Clearwater, Florida + 20 more", "locations": [ { "city": "Huntsville", "state": "Alabama" }, { "city": "San Diego", "state": "California" }, { "city": "Clearwater", "state": "Florida" }, { "city": "Orlando", "state": "Florida" }, { "city": "Decatur", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT00486512" }, { "nct_id": "NCT03420794", "title": "Optimization of Pre-operative Oral Analgesics in Patients Undergoing Ambulatory Minimally Invasive Hysterectomy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hysterectomy", "Laparoscopy", "Analgesia" ], "interventions": [ { "name": "Timing of pre-operative oral non-narcotic analgesics in relation to minimally invasive hysterectomy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 58, "start_date": "2018-01-12", "completion_date": "2021-12-01", "has_results": false, "last_update_posted_date": "2023-03-08", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 1, "location_summary": "Weston, Florida", "locations": [ { "city": "Weston", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03420794" }, { "nct_id": "NCT07787572", "title": "Applying Neuromodulation to Boost the Efficacy of Motivational Interviewing", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cannabis Use Disorder" ], "interventions": [ { "name": "transcranial alternating current stimulation", "type": "DEVICE" }, { "name": "sham transcranial alternating current stimulation", "type": "DEVICE" }, { "name": "Motivational interviewing (MI)", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "The Mind Research Network", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "21 Years to 65 Years" }, "enrollment_count": 82, "start_date": "2026-08", "completion_date": "2028-08", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 1, "location_summary": "Albuquerque, New Mexico", "locations": [ { "city": "Albuquerque", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT07787572" }, { "nct_id": "NCT01842802", "title": "Clinical Investigation of Non Invasive Fat Reduction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Subcutaneous Fat" ], "interventions": [ { "name": "Diode Laser", "type": "DEVICE" }, { "name": "YAG laser", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Cynosure, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "20 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "20 Years to 60 Years" }, "enrollment_count": 8, "start_date": "2012-01", "completion_date": "2013-08", "has_results": false, "last_update_posted_date": "2020-10-28", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 1, "location_summary": "Staten Island, New York", "locations": [ { "city": "Staten Island", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01842802" }, { "nct_id": "NCT03433339", "title": "Spinal Cord Stimulation for the Treatment of Major Depressive Disorder", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Major Depressive Disorder" ], "interventions": [ { "name": "Active transcutaneous spinal direct current stimulation", "type": "DEVICE" }, { "name": "Sham transcutaneous spinal direct current stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Cincinnati", "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": 20, "start_date": "2018-08-29", "completion_date": "2022-09-13", "has_results": true, "last_update_posted_date": "2024-12-27", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 1, "location_summary": "Mason, Ohio", "locations": [ { "city": "Mason", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03433339" }, { "nct_id": "NCT06979466", "title": "Q Therapeutic System for Chronic Stroke Recovery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Hemorrhage", "Brain Injury", "Cerebrovascular Accident (CVA)", "Chronic Stroke Patient" ], "interventions": [ { "name": "Q Therapeutic System (BQ 3.0) - Active", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Burke Rehabilitation Hospital", "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": 25, "start_date": "2025-05-26", "completion_date": "2026-06-30", "has_results": false, "last_update_posted_date": "2025-08-12", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 1, "location_summary": "White Plains, New York", "locations": [ { "city": "White Plains", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06979466" }, { "nct_id": "NCT02250092", "title": "Brain Stimulation and Hand Training in Children With Hemiparesis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pediatric Hemiparesis" ], "interventions": [ { "name": "Transcranial Direct Current Stimulation (tDCS)", "type": "DEVICE" }, { "name": "Placebo Comparator", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "8 Years to 21 Years" }, "enrollment_count": 20, "start_date": "2014-12-31", "completion_date": "2017-07-10", "has_results": true, "last_update_posted_date": "2020-08-18", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 2, "location_summary": "Minneapolis, Minnesota • Saint Paul, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" }, { "city": "Saint Paul", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02250092" }, { "nct_id": "NCT02735707", "title": "Randomized, Embedded, Multifactorial Adaptive Platform Trial for Community- Acquired Pneumonia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Community-acquired Pneumonia, Influenza, COVID-19" ], "interventions": [ { "name": "Ceftriaxone", "type": "DRUG" }, { "name": "Moxifloxacin or Levofloxacin", "type": "DRUG" }, { "name": "Piperacillin-tazobactam", "type": "DRUG" }, { "name": "Ceftaroline", "type": "DRUG" }, { "name": "Amoxicillin-clavulanate", "type": "DRUG" }, { "name": "Standard course macrolide", "type": "DRUG" }, { "name": "Extended course macrolide", "type": "DRUG" }, { "name": "No systemic corticosteroid", "type": "OTHER" }, { "name": "Fixed-duration Hydrocortisone", "type": "DRUG" }, { "name": "Shock-dependent hydrocortisone", "type": "DRUG" }, { "name": "Fixed-duration higher dose Hydrocortisone", "type": "DRUG" }, { "name": "No antiviral agent for influenza", "type": "OTHER" }, { "name": "Five-days oseltamivir", "type": "DRUG" }, { "name": "Ten-days oseltamivir", "type": "DRUG" }, { "name": "No antiviral agent for COVID-19", "type": "OTHER" }, { "name": "Lopinavir / Ritonavir", "type": "DRUG" }, { "name": "Hydroxychloroquine", "type": "DRUG" }, { "name": "Hydroxychloroquine + lopinavir/ritonavir", "type": "DRUG" }, { "name": "Ivermectin", "type": "DRUG" }, { "name": "No immune modulation for COVID-19", "type": "OTHER" }, { "name": "Interferon beta-1a", "type": "DRUG" }, { "name": "Anakinra", "type": "DRUG" }, { "name": "Tocilizumab", "type": "DRUG" }, { "name": "Sarilumab", "type": "DRUG" }, { "name": "Local standard venous thromboprophylaxis", "type": "DRUG" }, { "name": "Therapeutic dose anticoagulation", "type": "DRUG" }, { "name": "Conventional low dose thromboprophylaxis", "type": "DRUG" }, { "name": "Intermediate dose thromboprophylaxis", "type": "DRUG" }, { "name": "Continuation of therapeutic dose anticoagulation", "type": "DRUG" }, { "name": "No immunoglobulin", "type": "OTHER" }, { "name": "Convalescent plasma", "type": "BIOLOGICAL" }, { "name": "Delayed administration of convalescent plasma", "type": "BIOLOGICAL" }, { "name": "No vitamin C", "type": "OTHER" }, { "name": "Vitamin C", "type": "DRUG" }, { "name": "No antiplatelet", "type": "OTHER" }, { "name": "Aspirin", "type": "DRUG" }, { "name": "P2Y12 inhibitor", "type": "DRUG" }, { "name": "No simvastatin", "type": "OTHER" }, { "name": "Simvastatin", "type": "DRUG" }, { "name": "Eritoran", "type": "DRUG" }, { "name": "Apremilast", "type": "DRUG" }, { "name": "Clinician-preferred mechanical ventilation strategy", "type": "PROCEDURE" }, { "name": "Protocolised mechanical ventilation strategy", "type": "PROCEDURE" }, { "name": "No renin-angiotensin system inhibitor", "type": "OTHER" }, { "name": "Angiotensin converting enzyme inhibitor", "type": "DRUG" }, { "name": "Angiotensin Receptor Blockers", "type": "DRUG" }, { "name": "ARB + DMX-200", "type": "DRUG" }, { "name": "No cysteamine", "type": "OTHER" }, { "name": "Cysteamine", "type": "DRUG" }, { "name": "Fixed-duration dexamethasone", "type": "DRUG" }, { "name": "Baloxavir Marboxil", "type": "DRUG" }, { "name": "Five-days oseltamivir + baloxavir marboxil", "type": "DRUG" }, { "name": "Ten-days oseltamivir + baloxavir marboxil", "type": "DRUG" }, { "name": "No endothelial modulator", "type": "OTHER" }, { "name": "Imatinib", "type": "DRUG" }, { "name": "No Immune Modulator for Influenza", "type": "OTHER" }, { "name": "Baricitinib", "type": "DRUG" }, { "name": "Nirmatrelvir/ritonavir", "type": "DRUG" }, { "name": "Remdesivir", "type": "DRUG" }, { "name": "Nirmatrelvir/ritonavir + remdesivir", "type": "DRUG" } ], "intervention_types": [ "DRUG", "OTHER", "BIOLOGICAL", "PROCEDURE" ], "sponsor": "UMC Utrecht", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20000, "start_date": "2016-04-11", "completion_date": "2028-02", "has_results": false, "last_update_posted_date": "2024-07-12", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 11, "location_summary": "Jacksonville, Florida • Augusta, Georgia • Chicago, Illinois + 8 more", "locations": [ { "city": "Jacksonville", "state": "Florida" }, { "city": "Augusta", "state": "Georgia" }, { "city": "Chicago", "state": "Illinois" }, { "city": "New Orleans", "state": "Louisiana" }, { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT02735707" }, { "nct_id": "NCT05964699", "title": "The Use of a Non-Incised Minimally Invasive Flap Procedure in Conjunction With Emdogain® MI Compared to Traditional SRCP", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Periodontitis", "Attachment Loss, Periodontal" ], "interventions": [ { "name": "Minimally invasive periodontal therapy with use of Emdogain", "type": "PROCEDURE" }, { "name": "Minimally invasive periodontal therapy without the use of Emdogain", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Texas A&M University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "30 Years to 75 Years" }, "enrollment_count": 32, "start_date": "2023-07-31", "completion_date": "2025-07-31", "has_results": false, "last_update_posted_date": "2024-08-21", "last_synced_at": "2026-09-09T18:23:50.978Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05964699" } ] }