{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+applicator&page=33", "query": { "intervention": "Standard applicator", "page": 33 }, "page_size": 10 }, "pagination": { "page": 33, "page_size": 10, "total_count": 964, "total_pages": 97, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+applicator&page=34&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+applicator&page=32&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-02T18:21:21.203Z", "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": "NCT04318340", "title": "A Novel Tapered Applicator for Vaginal Vault Brachytherapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Endometrial Cancer", "Brachytherapy", "Quality of Life" ], "interventions": [ { "name": "Tapered applicator", "type": "OTHER" }, { "name": "Standard applicator", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Yale University", "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": 21, "start_date": "2020-07-16", "completion_date": "2023-03-20", "has_results": false, "last_update_posted_date": "2023-07-14", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT04318340" }, { "nct_id": "NCT01421641", "title": "Tenaculum Pain Control Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cervical Pain", "Pelvic Pain" ], "interventions": [ { "name": "Intracervical Lidocaine Injection", "type": "DRUG" }, { "name": "Topical Lidocaine Gel", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Oregon Health and Science University", "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": 74, "start_date": "2011-09", "completion_date": "2012-05", "has_results": true, "last_update_posted_date": "2014-04-21", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT01421641" }, { "nct_id": "NCT04240626", "title": "Multimodal Analgesia Effect on Post Surgical Patient", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Obesity, Morbid", "Surgery", "Bariatric Surgery Candidate" ], "interventions": [ { "name": "Neurontin", "type": "DRUG" }, { "name": "Dilaudid Injectable Product", "type": "DRUG" }, { "name": "Marcaine Injectable Product", "type": "DRUG" }, { "name": "Oxycodone Hydrochloride", "type": "DRUG" }, { "name": "Hycet 7.5Mg-325Mg/15Ml Solution", "type": "DRUG" }, { "name": "Zofran Injection", "type": "DRUG" }, { "name": "Scopolamine patch", "type": "DRUG" }, { "name": "Ativan", "type": "DRUG" }, { "name": "Flexeril Oral Product", "type": "DRUG" }, { "name": "Tylenol Suspension", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, Davis", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "35 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "35 Years to 65 Years · Female only" }, "enrollment_count": 60, "start_date": "2021-01-20", "completion_date": "2025-06-24", "has_results": false, "last_update_posted_date": "2026-09-14", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 1, "location_summary": "Sacramento, California", "locations": [ { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04240626" }, { "nct_id": "NCT00005774", "title": "Early Surfactant to Reduce Use of Mechanical Breathing in Low Birth Weight Infants", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Infant, Newborn", "Respiratory Distress Syndrome", "Respiratory Insufficiency" ], "interventions": [ { "name": "Early surfactant", "type": "DRUG" }, { "name": "Standard practice", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "NICHD Neonatal Research Network", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "12 Hours", "sex": "ALL", "summary": "Up to 12 Hours" }, "enrollment_count": 61, "start_date": "2000-05", "completion_date": "2002-07", "has_results": false, "last_update_posted_date": "2015-06-08", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 13, "location_summary": "Birmingham, Alabama • Palo Alto, California • New Haven, Connecticut + 10 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Palo Alto", "state": "California" }, { "city": "New Haven", "state": "Connecticut" }, { "city": "Miami", "state": "Florida" }, { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT00005774" }, { "nct_id": "NCT06707090", "title": "Tissue Repair Gel in Venous Leg Ulcers (US)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Venous Leg Ulcer", "Venous Ulcer", "Venous Stasis Ulcer", "Venous Stasis", "Wound Heal", "Wounds", "Venous Insufficiency of Leg", "Non-healing Wound" ], "interventions": [ { "name": "TR987 0.1% gel + Standard of Care", "type": "DRUG" }, { "name": "Standard of care", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "TR Therapeutics", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 312, "start_date": "2025-01-28", "completion_date": "2028-02", "has_results": false, "last_update_posted_date": "2026-02-12", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 33, "location_summary": "Tucson, Arizona • Castro Valley, California • Fresno, California + 27 more", "locations": [ { "city": "Tucson", "state": "Arizona" }, { "city": "Castro Valley", "state": "California" }, { "city": "Fresno", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06707090" }, { "nct_id": "NCT02904278", "title": "Novel Mobile Device Application to Improve Adherence", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pediatric Heart Transplant Recipients", "Pediatric Cardiac Transplantation", "Pediatric Heart Transplantation" ], "interventions": [ { "name": "Teen Pocket PATH® Mobile Application", "type": "OTHER" }, { "name": "Control Group: Standard of Care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "National Institute of Allergy and Infectious Diseases (NIAID)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "11 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "11 Years to 17 Years" }, "enrollment_count": 26, "start_date": "2017-08-10", "completion_date": "2019-11-01", "has_results": false, "last_update_posted_date": "2019-12-04", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 8, "location_summary": "Atlanta, Georgia • Boston, Massachusetts • St Louis, Missouri + 4 more", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "St Louis", "state": "Missouri" }, { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02904278" }, { "nct_id": "NCT06266650", "title": "Unilateral vs Bilateral Application of Muscle Energy Techniques in Pelvic Somatic Dysfunction", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pelvic Somatic Dysfunction" ], "interventions": [ { "name": "Osteopathic Treatment Technique- Muscle Energy Treatment", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Touro College and University System", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 100, "start_date": "2024-10-30", "completion_date": "2025-09-30", "has_results": false, "last_update_posted_date": "2024-12-03", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 1, "location_summary": "Harlem, New York", "locations": [ { "city": "Harlem", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06266650" }, { "nct_id": "NCT02996435", "title": "Smartphones to Improve Rivaroxaban ADHEREnce in Atrial Fibrillation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Atrial Fibrillation" ], "interventions": [ { "name": "Mobile Application Intervention", "type": "BEHAVIORAL" }, { "name": "No Intervention", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Janssen Scientific Affairs, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 139, "start_date": "2016-12-21", "completion_date": "2018-03-22", "has_results": false, "last_update_posted_date": "2018-10-26", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 25, "location_summary": "Anchorage, Alaska • Los Angeles, California • Manhattan Beach, California + 22 more", "locations": [ { "city": "Anchorage", "state": "Alaska" }, { "city": "Los Angeles", "state": "California" }, { "city": "Manhattan Beach", "state": "California" }, { "city": "Oakland", "state": "California" }, { "city": "Pasadena", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02996435" }, { "nct_id": "NCT07214597", "title": "NICU Utilization of Remote Voice Technology to Improve mateRnal Experience (NURTURE)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postpartum Depression (PPD)", "Self-Efficacy", "Parental Anxiety", "Engagement, Patient", "Usability", "Length of Stay" ], "interventions": [ { "name": "VoiceLove mobile phone application", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Vanderbilt University Medical Center", "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": 150, "start_date": "2026-02-04", "completion_date": "2028-01", "has_results": false, "last_update_posted_date": "2026-06-17", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT07214597" }, { "nct_id": "NCT06119425", "title": "Blood-Based Colorectal Cancer (CRC) Screening Implementation Into Clinical Practice Highlands", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer Colon" ], "interventions": [ { "name": "blood-based CRC screening", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Ballad Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": "84 Years", "sex": "ALL", "summary": "45 Years to 84 Years" }, "enrollment_count": 231, "start_date": "2023-10-12", "completion_date": "2025-04-30", "has_results": false, "last_update_posted_date": "2026-02-10", "last_synced_at": "2026-11-02T18:21:21.203Z", "location_count": 1, "location_summary": "Johnson City, Tennessee", "locations": [ { "city": "Johnson City", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT06119425" } ] }