{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+applicator&page=22", "query": { "intervention": "Standard applicator", "page": 22 }, "page_size": 10 }, "pagination": { "page": 22, "page_size": 10, "total_count": 963, "total_pages": 97, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+applicator&page=23&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+applicator&page=21&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-30T20:09:46.294Z", "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": "NCT03711149", "title": "Activity Monitor Feedback and Interactive Tours to Improve Postoperative Ambulation", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgery" ], "interventions": [ { "name": "Activity monitor feedback loop", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Cedars-Sinai Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 192, "start_date": "2018-12-05", "completion_date": "2019-12-30", "has_results": false, "last_update_posted_date": "2019-03-29", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03711149" }, { "nct_id": "NCT03762889", "title": "Peri-operative Application of Eyeprotx General Anesthesia Goggles As Prevention Against Corneal Injury Post Intubation.", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Corneal Injuries" ], "interventions": [ { "name": "Eyeprotx™ General Anesthesia Protective Goggles", "type": "DEVICE" }, { "name": "Eyelid Tape", "type": "DEVICE" }, { "name": "Eye Ointment", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": true, "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": "2019-06-06", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03762889" }, { "nct_id": "NCT05441579", "title": "Recruitment and Behavioral Economic Strategies", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Surgery", "Adolescent Behavior" ], "interventions": [ { "name": "Behavioral Economics (BE) recruitment strategies", "type": "BEHAVIORAL" }, { "name": "Biofeedback-based virtual reality (VR-BF)", "type": "OTHER" }, { "name": "Manage My Pain", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Vanessa Olbrecht", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "12 Years to 18 Years" }, "enrollment_count": 128, "start_date": "2022-05-17", "completion_date": "2022-09-08", "has_results": true, "last_update_posted_date": "2024-12-20", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05441579" }, { "nct_id": "NCT01888003", "title": "The Benefits of a Preoperative Anemia Management Program", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anemia, Iron-Deficiency" ], "interventions": [ { "name": "Iron sucrose", "type": "DRUG" }, { "name": "Epoetin Alfa", "type": "DRUG" }, { "name": "Blood Transfusion", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "19 Years to 80 Years" }, "enrollment_count": 51, "start_date": "2013-04", "completion_date": "2015-01", "has_results": true, "last_update_posted_date": "2015-05-28", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT01888003" }, { "nct_id": "NCT05070754", "title": "Cold Atmospheric Plasma Device for Pediatric Molluscum and Verruca", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Verruca Vulgaris", "Molluscum Contagiosum Skin Infection" ], "interventions": [ { "name": "Floating electrode-dielectric barrier device (FE-DBD) cold atmospheric plasma (CAP)", "type": "DEVICE" }, { "name": "Cryotherapy", "type": "DEVICE" }, { "name": "Canthardin Collodion", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "4 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "4 Years to 21 Years" }, "enrollment_count": 17, "start_date": "2021-12-02", "completion_date": "2022-12-31", "has_results": true, "last_update_posted_date": "2024-04-05", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05070754" }, { "nct_id": "NCT07077070", "title": "Investigating Electrical Categorical Loudness Scaling Using a Mobile Research App in Experienced Adult Cochlear Implant Participants", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hearing Loss, Sensorineural" ], "interventions": [ { "name": "Standard Electrical Categorical Loudness Scaling task (Standard-ELS)", "type": "DEVICE" }, { "name": "Fast Electrical Categorical Loudness Scaling task (Fast-ELS)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Cochlear", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2025-10-21", "completion_date": "2025-12-24", "has_results": false, "last_update_posted_date": "2026-01-08", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Lone Tree, Colorado", "locations": [ { "city": "Lone Tree", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT07077070" }, { "nct_id": "NCT04495946", "title": "Implementation and Effectiveness of Engagement and Collaborative Management to Proactively Advance Sepsis Survivorship", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sepsis" ], "interventions": [ { "name": "Sepsis Transition and Recovery (STAR) program", "type": "BEHAVIORAL" }, { "name": "Usual care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3894, "start_date": "2020-07-01", "completion_date": "2024-04-01", "has_results": true, "last_update_posted_date": "2025-09-19", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Charlotte, North Carolina", "locations": [ { "city": "Charlotte", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04495946" }, { "nct_id": "NCT03673566", "title": "Clinical Evaluation of the \"NICU Clinical Decision Support Dashboard\" - CHMCO", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Preterm Birth", "Low; Birthweight, Extremely (999 Grams or Less)", "Neonatal Infection", "Satisfaction", "Stress", "Chronic Lung Disease", "Growth Acceleration", "Adverse Event" ], "interventions": [ { "name": "NICU Dashboard", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Philips Healthcare", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 0, "start_date": "2019-03-20", "completion_date": "2020-04-01", "has_results": false, "last_update_posted_date": "2020-09-24", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "Omaha, Nebraska", "locations": [ { "city": "Omaha", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT03673566" }, { "nct_id": "NCT06552481", "title": "A Case-Control Study of Negative Pressure Platform Wound Devices (NP-PWD) for Skin and Soft Tissue Defects", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Skin Wound", "Soft Tissue Injuries" ], "interventions": [ { "name": "NP-PWD", "type": "DEVICE" }, { "name": "Wound Vac", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The Metis Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 28, "start_date": "2023-08-16", "completion_date": "2024-04-25", "has_results": false, "last_update_posted_date": "2024-08-14", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06552481" }, { "nct_id": "NCT03292601", "title": "Brace Monitoring for Adolescent Idiopathic Scoliosis (AIS)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Adolescent Idiopathic Scoliosis" ], "interventions": [ { "name": "NYRC Brace Scoliosis Monitor", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "17 Years", "sex": "FEMALE", "summary": "8 Years to 17 Years · Female only" }, "enrollment_count": 87, "start_date": "2017-10-18", "completion_date": "2027-02", "has_results": false, "last_update_posted_date": "2026-04-03", "last_synced_at": "2026-10-30T20:09:46.294Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03292601" } ] }