{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Propofol+Anesthesia&page=6", "query": { "intervention": "Propofol Anesthesia", "page": 6 }, "page_size": 10 }, "pagination": { "page": 6, "page_size": 10, "total_count": 196, "total_pages": 20, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Propofol+Anesthesia&page=7&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Propofol+Anesthesia&page=5&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-14T21:13:43.030Z", "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": "NCT05252858", "title": "A Pilot Study Investigating the nCAP Signal Relief Patch in Subjects Undergoing Primary Hip or Knee Replacement Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid Use", "Pain, Post Operative" ], "interventions": [ { "name": "nCAP Signal Relief Patch", "type": "DEVICE" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Jacques E. Chelly", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 79, "start_date": "2022-03-21", "completion_date": "2022-10-08", "has_results": true, "last_update_posted_date": "2024-04-18", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05252858" }, { "nct_id": "NCT07829458", "title": "The Use of Remimazolam for TEE", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cardiac Disease", "Anesthesia" ], "interventions": [ { "name": "Remimazolam", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Icahn School of Medicine at Mount Sinai", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 210, "start_date": "2026-09", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2026-09-21", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07829458" }, { "nct_id": "NCT03540030", "title": "Opioid-Free Shoulder Arthroplasty", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Use", "Shoulder Osteoarthritis", "Avascular Necrosis", "Rotator Cuff Tear", "Arthritis;Inflammatory" ], "interventions": [ { "name": "Gabapentin", "type": "DRUG" }, { "name": "Celecoxib", "type": "DRUG" }, { "name": "toradol", "type": "DRUG" }, { "name": "acetaminophen", "type": "DRUG" }, { "name": "regional block", "type": "DRUG" }, { "name": "propofol", "type": "DRUG" }, { "name": "IV lidocaine", "type": "DRUG" }, { "name": "rocuronium", "type": "DRUG" }, { "name": "vecuronium", "type": "DRUG" }, { "name": "sevoflurane", "type": "DRUG" }, { "name": "desflurane", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "OrthoCarolina Research Institute, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 86, "start_date": "2016-09", "completion_date": "2019-06", "has_results": true, "last_update_posted_date": "2020-10-14", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "Charlotte, North Carolina", "locations": [ { "city": "Charlotte", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03540030" }, { "nct_id": "NCT05486416", "title": "Safety and Efficacy of HSK3486 Compared to Propofol for Induction of General Anesthesia in Adults With Elective Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "General Anesthesia" ], "interventions": [ { "name": "HSK3486", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Haisco-USA Pharmaceuticals, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 465, "start_date": "2024-01-12", "completion_date": "2024-07-23", "has_results": true, "last_update_posted_date": "2025-10-10", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 21, "location_summary": "Florence, Alabama • Sheffield, Alabama • Miami, Florida + 15 more", "locations": [ { "city": "Florence", "state": "Alabama" }, { "city": "Sheffield", "state": "Alabama" }, { "city": "Miami", "state": "Florida" }, { "city": "Sarasota", "state": "Florida" }, { "city": "Tamarac", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05486416" }, { "nct_id": "NCT03962725", "title": "Avoiding Neuromuscular Blockers to Reduce Complications", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Respiratory Failure", "Respiratory Infection", "Aspiration Pneumonia", "Pneumonitis", "Atelectasis", "Bronchospasm" ], "interventions": [ { "name": "Neuromuscular Blocking Agents", "type": "DRUG" }, { "name": "Anesthetic Adjuncts", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Beth Israel Deaconess 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": 3, "start_date": "2019-08-07", "completion_date": "2022-12-19", "has_results": true, "last_update_posted_date": "2026-06-04", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 2, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03962725" }, { "nct_id": "NCT01736020", "title": "Developing Anesthesia as Post Traumatic Stress Disorder (PTSD) Therapy", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Healthy" ], "interventions": [ { "name": "Dexmedetomidine", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" }, { "name": "Ketamine", "type": "DRUG" }, { "name": "Nitrous Oxide", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Southern California Institute for Research and Education", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "18 Years to 35 Years" }, "enrollment_count": 293, "start_date": "2009-09", "completion_date": "2017-04", "has_results": false, "last_update_posted_date": "2016-10-13", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "Irvine, California", "locations": [ { "city": "Irvine", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01736020" }, { "nct_id": "NCT03173326", "title": "Patient Satisfaction and Postoperative Analgesia Between Subarachnoid Block With 2-chloroprocaine Versus General Anesthesia for Knee Arthroscopy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Knee Arthroscopy", "General Anesthesia", "Subarachnoid Block" ], "interventions": [ { "name": "General anesthesia", "type": "PROCEDURE" }, { "name": "Subarachnoid block", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "30 Years to 65 Years" }, "enrollment_count": 1, "start_date": "2017-06-16", "completion_date": "2018-04-20", "has_results": false, "last_update_posted_date": "2018-08-08", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT03173326" }, { "nct_id": "NCT07001267", "title": "Prospective Randomized Observer Blinded Single Center Study Comparing 90-day Functional Outcome in Patients Who Received Intravenous Propofol Infusion Versus Inhalational Sevoflurane for General Anesthesia During Mechanical Thrombectomy in Patients Who Suffered From Acute Ischemic Stroke", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Ischemic Stroke Patients" ], "interventions": [ { "name": "Anesthesia drugs during the surgery", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Kansas 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": 120, "start_date": "2025-06-04", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-03-12", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "Kansas City, Kansas", "locations": [ { "city": "Kansas City", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07001267" }, { "nct_id": "NCT04947397", "title": "Investigation of Pupillometry as Guide for Extubation Readiness in Anesthetized Children", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anesthesia", "Laryngospasm on Emergence" ], "interventions": [ { "name": "Pupillometry", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": "10 Years", "sex": "ALL", "summary": "2 Years to 10 Years" }, "enrollment_count": 20, "start_date": "2022-06-20", "completion_date": "2023-02-01", "has_results": true, "last_update_posted_date": "2025-01-22", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "Oakland, California", "locations": [ { "city": "Oakland", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04947397" }, { "nct_id": "NCT02164929", "title": "Comparison Study of Transversus Abdominal Plane, Paravertebral and Epidural Blocks in Laparoscopic Colectomy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Laparoscopic Colorectal Resection" ], "interventions": [ { "name": "TAP block", "type": "PROCEDURE" }, { "name": "Epidural", "type": "PROCEDURE" }, { "name": "Paravertebral block", "type": "PROCEDURE" }, { "name": "Acetaminophen 1g IV", "type": "DRUG" }, { "name": "Dexamethasone 4mg", "type": "DRUG" }, { "name": "Midazolam up to 2mg", "type": "DRUG" }, { "name": "Propofol 1-2.5 mg/kg", "type": "DRUG" }, { "name": "Sevoflurane to keep a bispectral index of between 40-60", "type": "DRUG" }, { "name": "Local infiltration with 10 mL of plain ropivacaine 0.25%", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" }, { "name": "Epinephrine", "type": "DRUG" }, { "name": "Hydromorphone", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DRUG" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 17, "start_date": "2013-12", "completion_date": "2015-03", "has_results": true, "last_update_posted_date": "2017-09-25", "last_synced_at": "2026-10-14T21:13:43.030Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02164929" } ] }