{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sedation&page=2", "query": { "intervention": "Sedation", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sedation&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-12T07:29:19.993Z", "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": "NCT02501941", "title": "Spreading Depolarization and Ketamine Suppression", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Cortical Spreading Depolarization", "Cortical Spreading Depression", "Subarachoid Hemorrhage", "Traumatic Brain Injury" ], "interventions": [ { "name": "ketamine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of New Mexico", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 10, "start_date": "2015-07", "completion_date": "2017-05-01", "has_results": false, "last_update_posted_date": "2024-01-11", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Albuquerque, New Mexico", "locations": [ { "city": "Albuquerque", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT02501941" }, { "nct_id": "NCT02887157", "title": "Analyzing Retinal Microanatomy in ROP", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Retinopathy of Prematurity", "Neurodevelopmental Disorders", "Macular Edema" ], "interventions": [ { "name": "Swept Source OCT", "type": "DEVICE" }, { "name": "Magnetic Resonance Imaging", "type": "OTHER" }, { "name": "Scavenged blood collection", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Weeks", "maximum_age": null, "sex": "ALL", "summary": "30 Weeks and older" }, "enrollment_count": 191, "start_date": "2016-07-22", "completion_date": "2021-04-15", "has_results": false, "last_update_posted_date": "2023-02-10", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 4, "location_summary": "Gainesville, Florida • St Louis, Missouri • Durham, North Carolina + 1 more", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "St Louis", "state": "Missouri" }, { "city": "Durham", "state": "North Carolina" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02887157" }, { "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": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07672301" }, { "nct_id": "NCT07369128", "title": "Propofol-Only Versus Dexmedetomidine-Propofol in Children Undergoing Magnetic Resonance Imaging", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "MRI Sedation", "Pediatric Sedation", "Propofol Dosage", "Emergence Delirium, Anesthesia", "Recovery Time", "Dexmedetomidine" ], "interventions": [ { "name": "Dexmedetomidine (IV) 0.5 mcg/kg", "type": "DRUG" }, { "name": "Propofol (IV) 2-4 mg/kg", "type": "DRUG" }, { "name": "Dexmedetomidine (IV) 1 mcg/kg", "type": "DRUG" }, { "name": "Propofol (IV) 1-2 mg/kg", "type": "DRUG" }, { "name": "Propofol (IV) Infusion 250 mcg/kg/min", "type": "DRUG" }, { "name": "Propofol (IV) Infusion 150 mcg/kg/min", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Boston Children's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": "12 Years", "sex": "ALL", "summary": "1 Year to 12 Years" }, "enrollment_count": 105, "start_date": "2026-06", "completion_date": "2028-03", "has_results": false, "last_update_posted_date": "2026-05-29", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07369128" }, { "nct_id": "NCT02025855", "title": "Adjunct Methadone to Decrease the Duration of Mechanical Ventilation in the Medical Intensive Care Unit", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Use, Unspecified With Withdrawal", "Opioid-Induced Disorders", "Delirium" ], "interventions": [ { "name": "Methadone", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Henry Ford Health System", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 9, "start_date": "2014-01", "completion_date": "2017-10", "has_results": true, "last_update_posted_date": "2025-12-05", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT02025855" }, { "nct_id": "NCT01200433", "title": "The Effects of Dexmedetomidine and Propofol on Cerebral Blood Flow and Brain Oxygenation During Deep Brain Stimulation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Intracranial Neurosurgery" ], "interventions": [ { "name": "dexmedetomidine", "type": "DRUG" }, { "name": "propofol", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The Cleveland 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": "2013-08", "has_results": true, "last_update_posted_date": "2016-12-14", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01200433" }, { "nct_id": "NCT02751333", "title": "Esophageal Stent Migration With Endoscopic Suture Fixation Compared to Standard Deployment", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Esophageal Strictures", "Esophageal Leak", "Esophageal Perforation", "Esophageal Fistula", "Endostitch", "Esophageal Stent" ], "interventions": [ { "name": "FCSEMS with Endostitch (ES)", "type": "PROCEDURE" }, { "name": "FCSEMS with No Suturing (NS)", "type": "PROCEDURE" }, { "name": "Fully Covered Self-Expanding Metal Stents (FCSEMS)", "type": "DEVICE" }, { "name": "EndoStitch (ES) with the OverStitchTM system", "type": "DEVICE" } ], "intervention_types": [ "PROCEDURE", "DEVICE" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 0, "start_date": "2016-03", "completion_date": "2017-02", "has_results": false, "last_update_posted_date": "2017-05-15", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT02751333" }, { "nct_id": "NCT05148078", "title": "Pediatric Radiation Oncology With Movie Induced Sedation Effect (PROMISE)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Pediatric Cancer" ], "interventions": [ { "name": "PROMISE (Pediatric Radiation Oncology with Movie Induced Sedation Effect)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Texas Southwestern Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": "11 Years", "sex": "ALL", "summary": "3 Years to 11 Years" }, "enrollment_count": 30, "start_date": "2022-08-01", "completion_date": "2024-11-26", "has_results": true, "last_update_posted_date": "2026-03-02", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05148078" }, { "nct_id": "NCT00125424", "title": "Study of AQUAVAN® Injection (AQUAVAN; Fospropofol Disodium) for Sedation During Colonoscopy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Colonoscopy", "Colonic Polyps" ], "interventions": [ { "name": "AQUAVAN® (fospropofol disodium) Injection", "type": "DRUG" }, { "name": "Midazolam HCl", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Eisai Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 125, "start_date": "2005-07", "completion_date": "2005-09", "has_results": false, "last_update_posted_date": "2008-11-07", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 20, "location_summary": "Huntsville, Alabama • Phoenix, Arizona • Atlanta, Georgia + 16 more", "locations": [ { "city": "Huntsville", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Rockford", "state": "Illinois" }, { "city": "Evansville", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT00125424" }, { "nct_id": "NCT03525860", "title": "Acupuncture Treatment for Patients Who Develop Arrhythmias in the Post-Operative Cardio-Thoracic Setting", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-Operative Atrial Fibrillation", "Acupuncture Therapy" ], "interventions": [ { "name": "Acupuncture", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "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": 47, "start_date": "2018-07-26", "completion_date": "2019-08-26", "has_results": false, "last_update_posted_date": "2021-11-12", "last_synced_at": "2026-09-12T07:29:19.993Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03525860" } ] }