{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Anesthesia%2C+Intravenous&page=3", "query": { "condition": "Anesthesia, Intravenous", "page": 3 }, "page_size": 10 }, "pagination": { "page": 3, "page_size": 10, "total_count": 72, "total_pages": 8, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Anesthesia%2C+Intravenous&page=4&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Anesthesia%2C+Intravenous&page=2&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-01T03:59:39.123Z", "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": "NCT02469961", "title": "Dexmedetomidine vs Propofol TIVA (Total Intravenous Anesthesia) and Interscalene Block", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Shoulder Pain" ], "interventions": [ { "name": "Dexmedetomidine", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" }, { "name": "Interscalene block", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Maimonides Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "21 Years to 100 Years" }, "enrollment_count": 50, "start_date": "2010-10", "completion_date": "2012-07", "has_results": true, "last_update_posted_date": "2024-11-13", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Brooklyn, New York", "locations": [ { "city": "Brooklyn", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02469961" }, { "nct_id": "NCT06720415", "title": "Oral and Intravenous Methadone for Analgesia in Cardiac Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Anesthesia", "Cardiac Surgery" ], "interventions": [ { "name": "Oral methadone, immediately prior to transport", "type": "DRUG" }, { "name": "Intravenous methadone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 41, "start_date": "2025-04-14", "completion_date": "2025-07-14", "has_results": true, "last_update_posted_date": "2026-08-06", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06720415" }, { "nct_id": "NCT02086123", "title": "Randomized Study Comparing the Use of Epidural Analgesia to Intravenous Narcotics for Laparoscopic Colorectal Resection.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain, Postoperative" ], "interventions": [ { "name": "Epidural Analgesia", "type": "PROCEDURE" }, { "name": "Parenteral Analgesia (Intravenous)", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of California, Irvine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 87, "start_date": "2012-05", "completion_date": "2015-04", "has_results": false, "last_update_posted_date": "2023-08-14", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Orange, California", "locations": [ { "city": "Orange", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02086123" }, { "nct_id": "NCT05730920", "title": "IV Methadone Vs EXPAREL Erector Spinae Plane Blockade in Pediatric Subjects Undergoing Idiopathic Scoliosis Correction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Adolescent Idiopathic Scoliosis", "Juvenile Idiopathic Scoliosis" ], "interventions": [ { "name": "Methadone", "type": "DRUG" }, { "name": "Liposomal bupivacaine (LB, Exparel)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Dr. Casey Stondell, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "11 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "11 Years to 17 Years" }, "enrollment_count": 30, "start_date": "2022-10-19", "completion_date": "2024-09-21", "has_results": false, "last_update_posted_date": "2024-10-04", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Sacramento, California", "locations": [ { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05730920" }, { "nct_id": "NCT00615472", "title": "Intravenous Versus Inhalational Anesthesia in Parkinson's Disease", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Parkinson's Disease" ], "interventions": [ { "name": "Isoflurane", "type": "DRUG" }, { "name": "Remifentanil", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 58, "start_date": "2003-10", "completion_date": "2011-04", "has_results": true, "last_update_posted_date": "2015-07-13", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00615472" }, { "nct_id": "NCT04144153", "title": "Opioid Free Anesthesia and Bariatric Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Postoperative Quality of Recovery" ], "interventions": [ { "name": "Opioid Free Total Intravenous Anesthesia", "type": "COMBINATION_PRODUCT" }, { "name": "Total Intravenous anesthesia with opioid", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "Northwell Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 58, "start_date": "2021-08-09", "completion_date": "2023-09-01", "has_results": false, "last_update_posted_date": "2024-09-19", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04144153" }, { "nct_id": "NCT01377441", "title": "Effect of Intravenous Ibuprofen on Inflammatory Responses in Patients Undergoing Surgery With General Anesthesia.", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Inflammatory Response" ], "interventions": [ { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Placebo/Saline solution", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6, "start_date": "2011-09", "completion_date": "2013-05", "has_results": true, "last_update_posted_date": "2017-12-22", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 2, "location_summary": "Brooklyn, New York • New York, New York", "locations": [ { "city": "Brooklyn", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01377441" }, { "nct_id": "NCT07672301", "title": "Total Intravenous Anesthesia vs Spinal Anesthesia in Patients Undergoing Unilateral Primary Total Knee Arthroplasty", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Total Knee Arthroplasty (TKA)" ], "interventions": [ { "name": "Total IntraVenous Anesthesia (TIVA)", "type": "COMBINATION_PRODUCT" }, { "name": "Spinal-Block", "type": "COMBINATION_PRODUCT" }, { "name": "Electroencephalogram (EEG)", "type": "DEVICE" } ], "intervention_types": [ "COMBINATION_PRODUCT", "DEVICE" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 150, "start_date": "2026-03-11", "completion_date": "2028-06", "has_results": false, "last_update_posted_date": "2026-06-26", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07672301" }, { "nct_id": "NCT00444756", "title": "Jet Injection of 1% Buffered Lidocaine Versus Topical ELA-Max for Anesthesia Prior to Intravenous (IV) Catheterization in Children", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pain" ], "interventions": [ { "name": "J-tip jet injection of 1% buffered lidocaine", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Norton Healthcare", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "8 Years", "maximum_age": "15 Years", "sex": "ALL", "summary": "8 Years to 15 Years" }, "enrollment_count": 70, "start_date": "2005-04", "completion_date": "2006-04", "has_results": false, "last_update_posted_date": "2007-03-08", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT00444756" }, { "nct_id": "NCT05748626", "title": "Anti-Snoring Appliances and Airway Manipulation in Patients Undergoing Anesthetic Sedation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Airway Obstruction", "Snoring", "Sedation Complication" ], "interventions": [ { "name": "Anti-snoring device", "type": "DEVICE" }, { "name": "No anti -snoring device during their procedure.", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 25, "start_date": "2023-03-06", "completion_date": "2023-10-24", "has_results": true, "last_update_posted_date": "2025-08-14", "last_synced_at": "2026-10-01T03:59:39.123Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05748626" } ] }