{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Ringers+Lactate+or+Normal+Saline", "query": { "intervention": "Ringers Lactate or Normal Saline" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 31, "total_pages": 4, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Ringers+Lactate+or+Normal+Saline&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-26T14:42:50.628Z", "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": "NCT02726620", "title": "Decision Support for Intraoperative Low Blood Pressure", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypotension" ], "interventions": [ { "name": "Attending real-time decision support", "type": "PROCEDURE" }, { "name": "In-room real-time decision support", "type": "PROCEDURE" }, { "name": "Attending feedback emails", "type": "PROCEDURE" }, { "name": "In-room provider feedback emails", "type": "PROCEDURE" }, { "name": "Anesthesia Information Management System (AIMS)", "type": "DEVICE" }, { "name": "Perioperative Data Warehouse (PDW)", "type": "DEVICE" }, { "name": "General anesthesia", "type": "PROCEDURE" }, { "name": "Pager system", "type": "DEVICE" }, { "name": "Central neuraxial anesthesia", "type": "PROCEDURE" }, { "name": "Non-cardiac surgery", "type": "PROCEDURE" }, { "name": "Propofol", "type": "DRUG" }, { "name": "Sevoflurane", "type": "DRUG" }, { "name": "Desflurane", "type": "DRUG" }, { "name": "Isoflurane", "type": "DRUG" }, { "name": "Ephedrine", "type": "DRUG" }, { "name": "Phenylephrine", "type": "DRUG" }, { "name": "Norepinephrine", "type": "DRUG" }, { "name": "Epinephrine", "type": "DRUG" }, { "name": "Dobutamine", "type": "DRUG" }, { "name": "Dopamine", "type": "DRUG" }, { "name": "Isoproterenol", "type": "DRUG" }, { "name": "Milrinone", "type": "DRUG" }, { "name": "Atropine", "type": "DRUG" }, { "name": "Glycopyrrolate", "type": "DRUG" }, { "name": "Vasopressin", "type": "DRUG" }, { "name": "Terlipressin", "type": "DRUG" }, { "name": "Sodium Chloride 0.9%", "type": "DRUG" }, { "name": "Ringer's lactate", "type": "DRUG" }, { "name": "Hydroxyethyl starch solutions", "type": "DRUG" }, { "name": "Fresh Frozen Plasma", "type": "DRUG" }, { "name": "Packed Red Blood Cells", "type": "DRUG" }, { "name": "Albumin solutions", "type": "DRUG" }, { "name": "Plasma-Lyte", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" }, { "name": "Bupivacaine", "type": "DRUG" }, { "name": "Levobupivacaine", "type": "DRUG" }, { "name": "Ropivacaine", "type": "DRUG" }, { "name": "Mepivacaine", "type": "DRUG" }, { "name": "Tetracaine", "type": "DRUG" }, { "name": "Prilocaine", "type": "DRUG" }, { "name": "Procaine", "type": "DRUG" }, { "name": "Chloroprocaine", "type": "DRUG" }, { "name": "Benzocaine", "type": "DRUG" }, { "name": "Articaine", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DEVICE", "DRUG" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "60 Years to 100 Years" }, "enrollment_count": 22435, "start_date": "2017-01-05", "completion_date": "2018-12-29", "has_results": true, "last_update_posted_date": "2019-05-16", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02726620" }, { "nct_id": "NCT04651166", "title": "Effect of Prophylactic Tranexamic Acid on Bleeding Outcomes for Dilation and Evacuation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Abortion", "Dilation and Evacuation", "Hemorrhage", "Blood Loss" ], "interventions": [ { "name": "Tranexamic acid", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Hawaii", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": null, "sex": "FEMALE", "summary": "14 Years and older · Female only" }, "enrollment_count": 48, "start_date": "2022-02-15", "completion_date": "2023-07-27", "has_results": false, "last_update_posted_date": "2023-09-06", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 1, "location_summary": "Honolulu, Hawaii", "locations": [ { "city": "Honolulu", "state": "Hawaii" } ], "official_url": "https://clinicaltrials.gov/study/NCT04651166" }, { "nct_id": "NCT04450693", "title": "Cryopreserved Human Umbilical Cord (TTAX01) for Late Stage, Complex Non-healing Diabetic Foot Ulcers (AMBULATE DFU II)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Diabetic Foot Infection", "Non-healing Wound", "Non-healing Diabetic Foot Ulcer" ], "interventions": [ { "name": "TTAX01", "type": "BIOLOGICAL" }, { "name": "Standard care", "type": "OTHER" } ], "intervention_types": [ "BIOLOGICAL", "OTHER" ], "sponsor": "BioTissue Holdings, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 106, "start_date": "2020-11-20", "completion_date": "2025-03-24", "has_results": false, "last_update_posted_date": "2025-04-01", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 16, "location_summary": "Guntersville, Alabama • Tucson, Arizona • Los Angeles, California + 12 more", "locations": [ { "city": "Guntersville", "state": "Alabama" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Los Angeles", "state": "California" }, { "city": "Mather", "state": "California" }, { "city": "Palmdale", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04450693" }, { "nct_id": "NCT02444988", "title": "Isotonic Solutions and Major Adverse Renal Events Trial in the Medical Intensive Care Unit", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Critical Illness", "Acute Kidney Injury" ], "interventions": [ { "name": "0.9% Saline", "type": "OTHER" }, { "name": "Physiologically-balanced isotonic crystalloid", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Vanderbilt University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 5381, "start_date": "2015-06-01", "completion_date": "2017-06-30", "has_results": true, "last_update_posted_date": "2019-12-16", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02444988" }, { "nct_id": "NCT04364737", "title": "CONTAIN COVID-19: Convalescent Plasma to Limit COVID-19 Complications in Hospitalized Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "COVID-19", "Coronavirus", "Coronavirus Infection" ], "interventions": [ { "name": "Convalescent Plasma", "type": "BIOLOGICAL" }, { "name": "Saline solution", "type": "OTHER" } ], "intervention_types": [ "BIOLOGICAL", "OTHER" ], "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": 941, "start_date": "2020-04-17", "completion_date": "2022-12-12", "has_results": true, "last_update_posted_date": "2023-01-26", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 9, "location_summary": "New Haven, Connecticut • Miami, Florida • New York, New York + 5 more", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Miami", "state": "Florida" }, { "city": "New York", "state": "New York" }, { "city": "The Bronx", "state": "New York" }, { "city": "Edinburg", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04364737" }, { "nct_id": "NCT02565420", "title": "Saline Versus Lactated Ringer's Solution: The SOLAR Fluid Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Complications" ], "interventions": [ { "name": "Normal saline", "type": "OTHER" }, { "name": "Lactated Ringer's solution", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 8616, "start_date": "2015-09-28", "completion_date": "2019-01", "has_results": false, "last_update_posted_date": "2019-02-11", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02565420" }, { "nct_id": "NCT02083809", "title": "Effects of Oxytocin on Bleeding Outcomes During Dilation and Evacuation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Abortion", "Dilation and Evacuation", "Hemorrhage", "Blood Loss" ], "interventions": [ { "name": "intravenous oxytocin", "type": "DRUG" }, { "name": "Intravenous Fluids and Electrolytes", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Hawaii", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "14 Years to 50 Years · Female only" }, "enrollment_count": 166, "start_date": "2014-10", "completion_date": "2018-02", "has_results": true, "last_update_posted_date": "2020-11-27", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 2, "location_summary": "Honolulu, Hawaii • Seattle, Washington", "locations": [ { "city": "Honolulu", "state": "Hawaii" }, { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT02083809" }, { "nct_id": "NCT02548494", "title": "Early Administration of Long-acting Insulin Treatment of Diabetic Ketoacidosis in Pediatric Type 1 Diabetes", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus, Type 1", "Diabetic Ketoacidosis" ], "interventions": [ { "name": "Glargine", "type": "DRUG" }, { "name": "IV insulin", "type": "DRUG" }, { "name": "Electrolyte Correction", "type": "OTHER" }, { "name": "Correction of Fluid Loss", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Chattanooga-Hamilton County Hospital Authority", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Year", "maximum_age": "21 Years", "sex": "ALL", "summary": "1 Year to 21 Years" }, "enrollment_count": 17, "start_date": "2015-11", "completion_date": "2019-02-01", "has_results": false, "last_update_posted_date": "2020-09-23", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 1, "location_summary": "Chattanooga, Tennessee", "locations": [ { "city": "Chattanooga", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02548494" }, { "nct_id": "NCT04176120", "title": "Cryopreserved Human Umbilical Cord (TTAX01) for Late Stage, Complex Non-healing Diabetic Foot Ulcers (AMBULATE DFU)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Diabetic Foot Infection", "Non-healing Wound", "Non-healing Diabetic Foot Ulcer" ], "interventions": [ { "name": "TTAX01", "type": "BIOLOGICAL" }, { "name": "Standard Care", "type": "OTHER" } ], "intervention_types": [ "BIOLOGICAL", "OTHER" ], "sponsor": "BioTissue Holdings, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 220, "start_date": "2020-07-01", "completion_date": "2024-06-12", "has_results": false, "last_update_posted_date": "2024-06-14", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 16, "location_summary": "San Francisco, California • Sylmar, California • Miami, Florida + 13 more", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "Sylmar", "state": "California" }, { "city": "Miami", "state": "Florida" }, { "city": "West Palm Beach", "state": "Florida" }, { "city": "North Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04176120" }, { "nct_id": "NCT06418022", "title": "Evaluating Fluid Responsiveness in ICU Patients Using VTI and Trendelenburg Positioning", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shock", "Fluid Overload", "Cardiac Output, Low" ], "interventions": [ { "name": "Trendelenburg positioning VTI", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Lenox Hill Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 400, "start_date": "2024-04-01", "completion_date": "2025-08-01", "has_results": false, "last_update_posted_date": "2024-05-16", "last_synced_at": "2026-09-26T14:42:50.628Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06418022" } ] }