{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lazanda&page=18", "query": { "intervention": "Lazanda", "page": 18 }, "page_size": 10 }, "pagination": { "page": 18, "page_size": 10, "total_count": 475, "total_pages": 48, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lazanda&page=19&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Lazanda&page=17&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T05:31:28.189Z", "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": "NCT07269808", "title": "Sedation During Endoscopy Using Remimazolam: Efficacy in a Novel Exploration", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Anesthesia", "Sedation", "Endoscopy" ], "interventions": [ { "name": "Remimazolam", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Massachusetts General Hospital", "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": "2026-03-03", "completion_date": "2026-06-27", "has_results": false, "last_update_posted_date": "2026-09-14", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07269808" }, { "nct_id": "NCT01851720", "title": "Randomized Trial for Pain Management in Low-grade Subarachnoid Hemorrhage", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Headaches Associated With Subarachnoid Hemorrhage (SAH)" ], "interventions": [ { "name": "Low dose fentanyl PCA", "type": "DRUG" }, { "name": "Standard IV fentanyl bolus", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Johns Hopkins University", "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": 1, "start_date": "2012-07", "completion_date": "2014-09-15", "has_results": true, "last_update_posted_date": "2017-06-22", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01851720" }, { "nct_id": "NCT00807209", "title": "Dose Finding Posterolateral Thoracotomy Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "Low Dose SKY0402", "type": "DRUG" }, { "name": "High Dose SKY0402", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Fentanyl via PCA", "type": "DRUG" }, { "name": "Bupivacaine via epidural", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Pacira Pharmaceuticals, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3, "start_date": "2008-12", "completion_date": "2009-02", "has_results": true, "last_update_posted_date": "2012-05-15", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 5, "location_summary": "Pasadena, California • Orlando, Florida • Houston, Texas + 1 more", "locations": [ { "city": "Pasadena", "state": "California" }, { "city": "Orlando", "state": "Florida" }, { "city": "Houston", "state": "Texas" }, { "city": "Houston", "state": "Texas" }, { "city": "Tacoma", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT00807209" }, { "nct_id": "NCT02119806", "title": "Decreasing the Incidence of Delirium After Cardiac Surgery", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "C.Surgical Procedure; Cardiac", "Delirium" ], "interventions": [ { "name": "Benzodiazepine", "type": "DRUG" }, { "name": "Fentanyl", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, Los Angeles", "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": "2017-08", "completion_date": "2017-08", "has_results": false, "last_update_posted_date": "2018-06-12", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02119806" }, { "nct_id": "NCT01539538", "title": "A Multicenter, Randomized, Open-Label, Parallel-Group Trial to Compare the Efficacy and Safety of the Sufentanil NanoTab PCA System/15 mcg (Zalviso™)to Intravenous Patient-Controlled Analgesia With Morphine for the Treatment of Acute Post-Operative Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Post-Operative Pain" ], "interventions": [ { "name": "Sufentanil NanoTab PCA System/15 mcg", "type": "DRUG" }, { "name": "morphine IV PCA", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Talphera, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 357, "start_date": "2012-04", "completion_date": "2012-12", "has_results": true, "last_update_posted_date": "2015-10-01", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 16, "location_summary": "Florence, Alabama • Montgomery, Alabama • Sheffield, Alabama + 13 more", "locations": [ { "city": "Florence", "state": "Alabama" }, { "city": "Montgomery", "state": "Alabama" }, { "city": "Sheffield", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Pasadena", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01539538" }, { "nct_id": "NCT01701102", "title": "Study to Find Optimal Dose of Local Spinal Anesthetic (Mepivacaine) Combined With Narcotic (Fentanyl) For Knee Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Arthroscopic Knee Surgery" ], "interventions": [ { "name": "Mepivacaine (24 mg) plus fentanyl", "type": "PROCEDURE" }, { "name": "Mepivacaine (27 mg) plus fentanyl", "type": "PROCEDURE" }, { "name": "Mepivacaine (30 mg) plus fentanyl", "type": "PROCEDURE" }, { "name": "Mepivacaine", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Hospital for Special Surgery, New York", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 56, "start_date": "2011-12", "completion_date": "2013-12", "has_results": true, "last_update_posted_date": "2016-04-05", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01701102" }, { "nct_id": "NCT02532647", "title": "Safety and Efficacy of Remimazolam in ASA III and IV Patients Undergoing Colonoscopy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Colonoscopy" ], "interventions": [ { "name": "Remimazolam", "type": "DRUG" }, { "name": "Midazolam", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Paion UK Ltd.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 79, "start_date": "2015-11", "completion_date": "2016-12", "has_results": true, "last_update_posted_date": "2020-09-30", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 3, "location_summary": "Jupiter, Florida • Indianapolis, Indiana • Monroe, Louisiana", "locations": [ { "city": "Jupiter", "state": "Florida" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Monroe", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT02532647" }, { "nct_id": "NCT01810458", "title": "Liver Fibrosis in Alpha-1 Antitrypsin Deficiency (Liver AATD)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Liver Fibrosis", "Alpha-1 Antitrypsin Deficiency", "AAT Deficiency", "AATD" ], "interventions": [ { "name": "Abdominal ultrasound", "type": "DEVICE" }, { "name": "History and physical", "type": "PROCEDURE" }, { "name": "Intravenous catheter", "type": "PROCEDURE" }, { "name": "Blood draw", "type": "PROCEDURE" }, { "name": "Liver questionnaire", "type": "OTHER" }, { "name": "Liver Biopsy", "type": "PROCEDURE" }, { "name": "Midazolam", "type": "DRUG" }, { "name": "Fentanyl", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" }, { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Lorazepam", "type": "DRUG" }, { "name": "Oxycodone/Acetaminophen", "type": "DRUG" }, { "name": "Ondansetron", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "PROCEDURE", "OTHER", "DRUG" ], "sponsor": "University of Florida", "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": 109, "start_date": "2013-10", "completion_date": "2019-09", "has_results": false, "last_update_posted_date": "2023-08-21", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01810458" }, { "nct_id": "NCT00380978", "title": "Neuraxial Versus Systemic Analgesia for Latent Phase Labor Effect on Rate of Operative Delivery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Labor Pain", "Pregnancy" ], "interventions": [ { "name": "combined spinal epidural analgesia", "type": "PROCEDURE" }, { "name": "late analgesia (systemic)", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 1026, "start_date": "2001-10", "completion_date": "2008-09", "has_results": true, "last_update_posted_date": "2014-04-14", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT00380978" }, { "nct_id": "NCT04099030", "title": "Effect of Opioid Shortage on Drug Selection", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Opioid Use, Unspecified" ], "interventions": [], "intervention_types": [], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1668, "start_date": "2019-04-05", "completion_date": "2019-12-13", "has_results": false, "last_update_posted_date": "2020-04-16", "last_synced_at": "2026-10-23T05:31:28.189Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04099030" } ] }