{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?page=4&sponsor=Lahey+Clinic", "query": { "sponsor": "Lahey Clinic", "page": 4 }, "page_size": 10 }, "pagination": { "page": 4, "page_size": 10, "total_count": 77, "total_pages": 8, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?page=5&sponsor=Lahey+Clinic&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?page=3&sponsor=Lahey+Clinic&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-14T06:31:31.391Z", "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": "NCT01280617", "title": "Low Dose Thymoglobin in Renal Transplant Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Renal Failure" ], "interventions": [ { "name": "Thymoglobulin", "type": "DRUG" }, { "name": "Thymoglobulin 0.75mg/kg dose", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Lahey Clinic", "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": 44, "start_date": "2010-10", "completion_date": "2014-01", "has_results": true, "last_update_posted_date": "2021-03-16", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01280617" }, { "nct_id": "NCT00734136", "title": "Role Of Angiogenic Factors In The Development Of Hepatorenal Syndrome", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hepatorenal Syndrome", "Renal Failure", "Liver Diseases" ], "interventions": [ { "name": "Blood Draws and a hepatectomy specimen", "type": "PROCEDURE" }, { "name": "Blood draw - pre operative standard of care", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Lahey Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2005-05", "completion_date": "2009-02", "has_results": false, "last_update_posted_date": "2009-02-18", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00734136" }, { "nct_id": "NCT02524366", "title": "A Study of Transcorporal Versus Standard Artificial Urinary Sphincter Placement", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stress Urinary Incontinence" ], "interventions": [ { "name": "Artificial Urinary Sphincter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "MALE", "summary": "18 Years to 85 Years · Male only" }, "enrollment_count": 0, "start_date": "2015-09", "completion_date": "2017-11", "has_results": false, "last_update_posted_date": "2019-07-22", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02524366" }, { "nct_id": "NCT00808145", "title": "Study of Sorafenib, Gemcitabine, and Cisplatin in Advanced Hepatocellular Carcinoma (HCC)", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Hepatocellular Carcinoma" ], "interventions": [ { "name": "Gemcitabine / Cisplatin / Sorafenib", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Lahey Clinic", "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": 0, "start_date": "2009-02", "completion_date": "2014-10", "has_results": false, "last_update_posted_date": "2014-10-22", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00808145" }, { "nct_id": "NCT00872495", "title": "Evaluation of Non-Invasive Assays for the Detection of Urothelial Cancer", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Urothelial Cancer", "Cancer", "Bladder Neoplasms", "Urinary Bladder Cancer" ], "interventions": [], "intervention_types": [], "sponsor": "Lahey Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 500, "start_date": "2002-09", "completion_date": "2028-11", "has_results": false, "last_update_posted_date": "2025-12-08", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00872495" }, { "nct_id": "NCT00832065", "title": "Sexual Dysfunction And Hypotestosteronemia In Patients With Obstructive Sleep Apnea Syndrome", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Sleep Apnea, Obstructive", "Sleep Apnea", "Hypotestosteronism" ], "interventions": [], "intervention_types": [], "sponsor": "Lahey Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "MALE", "summary": "18 Years to 70 Years · Male only" }, "enrollment_count": 0, "start_date": "2009-01", "completion_date": "2016-08", "has_results": false, "last_update_posted_date": "2017-08-24", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 2, "location_summary": "Burlington, Massachusetts • Peabody, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" }, { "city": "Peabody", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00832065" }, { "nct_id": "NCT02431455", "title": "The Effect of Postoperative Incentive Spirometry on Pulmonary Function and Pulmonary Complications in Bariatric Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obesity, Morbid", "Complications of Bariatric Procedures", "Pulmonary Atelectasis", "Pneumonia" ], "interventions": [ { "name": "Incentive spirometer", "type": "DEVICE" }, { "name": "No incentive spirometer", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Lahey Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 224, "start_date": "2015-06", "completion_date": "2016-05", "has_results": true, "last_update_posted_date": "2016-08-25", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT02431455" }, { "nct_id": "NCT03936361", "title": "Statins In Intracerbral Hemorrhage", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Intracerebral Hemorrhage" ], "interventions": [ { "name": "Statins", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Beth Israel Deaconess Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 1456, "start_date": "2020-06-10", "completion_date": "2029-12", "has_results": false, "last_update_posted_date": "2026-04-21", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03936361" }, { "nct_id": "NCT00676455", "title": "Computer Assisted Volumetric Analysis of CT-Identified Metastatic Pulmonary Or Hepatic Lesions", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Metastatic Cancer" ], "interventions": [], "intervention_types": [], "sponsor": "Lahey Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 14, "start_date": "2007-02", "completion_date": "2009-01", "has_results": true, "last_update_posted_date": "2013-05-10", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00676455" }, { "nct_id": "NCT00695747", "title": "Intraocular Pressure Control Following One Site Versus Two Site Combined Phacoemulsification/IOL And Trabeculectomy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glaucoma", "Cataracts" ], "interventions": [ { "name": "2 Site procedure- Phacoemulsification/IOL and Trabeculectomy", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Lahey Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 95, "start_date": "1998-01", "completion_date": "2009-01", "has_results": false, "last_update_posted_date": "2009-01-22", "last_synced_at": "2026-10-14T06:31:31.391Z", "location_count": 1, "location_summary": "Burlington, Massachusetts", "locations": [ { "city": "Burlington", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00695747" } ] }