{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?page=4&sponsor=Northwell+Health", "query": { "sponsor": "Northwell Health", "page": 4 }, "page_size": 10 }, "pagination": { "page": 4, "page_size": 10, "total_count": 511, "total_pages": 52, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?page=5&sponsor=Northwell+Health&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?page=3&sponsor=Northwell+Health&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-17T01:31:40.610Z", "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": "NCT03414762", "title": "PICO Negative Pressure Wound Therapy in Obese Women Undergoing Elective Cesarean Delivery.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Cesarean Section Complications", "Cesarean Wound; Dehiscence", "Cesarean Wound Disruption" ], "interventions": [ { "name": "PICO Negative Pressure Wound Therapy", "type": "DEVICE" }, { "name": "Standard Dressing", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 153, "start_date": "2019-04-01", "completion_date": "2022-09-30", "has_results": false, "last_update_posted_date": "2024-02-29", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "New Hyde Park, New York", "locations": [ { "city": "New Hyde Park", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03414762" }, { "nct_id": "NCT01636375", "title": "Comparison of Muscle Atrophy After Direct Anterior & Posterior Total Hip Arthroplasty", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Osteoarthritis, Hip" ], "interventions": [], "intervention_types": [], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 19, "start_date": "2012-05", "completion_date": "2021-07", "has_results": false, "last_update_posted_date": "2021-11-19", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01636375" }, { "nct_id": "NCT06233812", "title": "Surgical Outcomes of Simple Interrupted Versus Running Epidermal Sutures in Full-thickness Skin Graft Placement", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Skin Graft Scar" ], "interventions": [ { "name": "Simple interrupted suturing technique", "type": "PROCEDURE" }, { "name": "Running suturing technique", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 52, "start_date": "2023-08-01", "completion_date": "2024-08-01", "has_results": false, "last_update_posted_date": "2024-01-31", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "North New Hyde Park, New York", "locations": [ { "city": "North New Hyde Park", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06233812" }, { "nct_id": "NCT03680872", "title": "Restoring Motor and Sensory Hand Function in Tetraplegia Using a Neural Bypass System", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries", "Spinal Cord Injury Cervical" ], "interventions": [ { "name": "Bidirectional Neural Bypass System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Chad Bouton", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "22 Years to 65 Years" }, "enrollment_count": 7, "start_date": "2019-09-30", "completion_date": "2028-12", "has_results": false, "last_update_posted_date": "2026-03-11", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03680872" }, { "nct_id": "NCT05389787", "title": "Impact of Cerebellar TMS on Brain and Cognitive Functions in Schizophrenia: a Pilot Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Schizophrenia", "Cerebellar Function", "Condition" ], "interventions": [ { "name": "Transcranial Magnetic Stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 40, "start_date": "2022-08-18", "completion_date": "2027-08-31", "has_results": false, "last_update_posted_date": "2025-09-25", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05389787" }, { "nct_id": "NCT02097251", "title": "An Open-Label Treatment Protocol With UX003 rhGUS Enzyme Replacement Therapy for an Advanced Stage MPS 7 Patient", "overall_status": "NO_LONGER_AVAILABLE", "study_type": "EXPANDED_ACCESS", "phases": [], "conditions": [ "Mucopolysaccharidosis Type 7" ], "interventions": [ { "name": "UX003", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Joyce Fox", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "MALE", "summary": "Male only" }, "enrollment_count": null, "start_date": null, "completion_date": null, "has_results": false, "last_update_posted_date": "2017-02-06", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "New Hyde Park, New York", "locations": [ { "city": "New Hyde Park", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02097251" }, { "nct_id": "NCT04782700", "title": "P-Co-Li (Pulmonary Covid-19 Study)", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Covid19", "Lung Inflammation", "Hypoxemic Respiratory Failure" ], "interventions": [ { "name": "Steroid Taper (Prednisone)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2021-04-01", "completion_date": "2021-06-08", "has_results": false, "last_update_posted_date": "2022-02-16", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04782700" }, { "nct_id": "NCT04256837", "title": "Effect of Transcutaneous Electrical Auricular Stimulation of the Vagus Nerve in Kidney Transplant Recipients", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Vagus Nerve Stimulation" ], "interventions": [ { "name": "Transcutaneous electrical auricular vagus nerve stimulation (VNS)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 47, "start_date": "2020-01-13", "completion_date": "2021-01-07", "has_results": false, "last_update_posted_date": "2022-12-14", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04256837" }, { "nct_id": "NCT05977946", "title": "Delivering Transcutaneous Auricular Neurostimulation to Regulate Platelet Activity in Healthy Human Subjects", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hemostasis", "Blood Biomarkers" ], "interventions": [ { "name": "Volta System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Spark Biomedical, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 25, "start_date": "2023-10-31", "completion_date": "2024-08-06", "has_results": false, "last_update_posted_date": "2025-04-09", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05977946" }, { "nct_id": "NCT00289367", "title": "Study of T3 on the Incidence of Atrial Fibrillation in Patients Undergoing Cardiac Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Atrial Fibrillation" ], "interventions": [ { "name": "triiodothyronine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 280, "start_date": "2006-02", "completion_date": "2008-05", "has_results": false, "last_update_posted_date": "2008-05-20", "last_synced_at": "2026-10-17T01:31:40.610Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00289367" } ] }