{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Clinical+Decision+Support+Tool&page=6", "query": { "intervention": "Clinical Decision Support Tool", "page": 6 }, "page_size": 10 }, "pagination": { "page": 6, "page_size": 10, "total_count": 272, "total_pages": 28, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Clinical+Decision+Support+Tool&page=7&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Clinical+Decision+Support+Tool&page=5&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-07T13:31:23.437Z", "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": "NCT04295135", "title": "Chronic Pain OneSheet Clinical Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Pain" ], "interventions": [ { "name": "Chronic Pain OneSheet", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 137, "start_date": "2020-08-04", "completion_date": "2022-05-18", "has_results": true, "last_update_posted_date": "2024-05-24", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 2, "location_summary": "Indianapolis, Indiana • Winston-Salem, North Carolina", "locations": [ { "city": "Indianapolis", "state": "Indiana" }, { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04295135" }, { "nct_id": "NCT03169868", "title": "Enhanced Medication Reconciliation For Serious Mental Illness", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mental Disorders" ], "interventions": [ { "name": "Sano Patient Medication Profile", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Precera Bioscience, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 26, "start_date": "2018-02-27", "completion_date": "2019-01-21", "has_results": false, "last_update_posted_date": "2019-01-25", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03169868" }, { "nct_id": "NCT03584789", "title": "De-Implementing Opioids for Dental Extractions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tooth Extraction" ], "interventions": [ { "name": "Clinical Decision Support", "type": "OTHER" }, { "name": "Patient education", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "HealthPartners Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "16 Years", "maximum_age": null, "sex": "ALL", "summary": "16 Years and older" }, "enrollment_count": 5722, "start_date": "2020-02-17", "completion_date": "2021-05-21", "has_results": true, "last_update_posted_date": "2022-08-30", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Bloomington, Minnesota", "locations": [ { "city": "Bloomington", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03584789" }, { "nct_id": "NCT04771208", "title": "I Kua na'u Advance Care Planning for Native Hawaiian Elders", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Advance Care Planning" ], "interventions": [ { "name": "I kua na'u \"Let Me Carry Out Your Last Wishes\"", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Tufts Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "55 Years", "maximum_age": null, "sex": "ALL", "summary": "55 Years and older" }, "enrollment_count": 220, "start_date": "2023-03-16", "completion_date": "2026-08-31", "has_results": false, "last_update_posted_date": "2026-03-16", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Honolulu, Hawaii", "locations": [ { "city": "Honolulu", "state": "Hawaii" } ], "official_url": "https://clinicaltrials.gov/study/NCT04771208" }, { "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": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02726620" }, { "nct_id": "NCT05745103", "title": "Optimizing Behavioral Healthcare Delivery Through Technology", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mood Disorders", "Anxiety Disorders" ], "interventions": [ { "name": "Cognitive behavioral therapy with AI", "type": "BEHAVIORAL" }, { "name": "Cognitive behavioral therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Eleos Health", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 46, "start_date": "2021-09-01", "completion_date": "2023-04-30", "has_results": false, "last_update_posted_date": "2024-01-31", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Joplin, Missouri", "locations": [ { "city": "Joplin", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05745103" }, { "nct_id": "NCT07438743", "title": "An Evaluation of Epic EHR AI Outpatient Chart Summarization", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Quality Improvement" ], "interventions": [ { "name": "GenAI Chart Summarization", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 284, "start_date": "2026-02-23", "completion_date": "2026-05", "has_results": false, "last_update_posted_date": "2026-03-06", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07438743" }, { "nct_id": "NCT07706920", "title": "Testing an AI Tool to Help Primary Care Clinicians With Specialty Consultation Questions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Decision Support Systems, Clinical", "Referral and Consultation" ], "interventions": [ { "name": "SAGE (AI clinical decision support)", "type": "OTHER" }, { "name": "Standard eConsult", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 16, "start_date": "2026-08-17", "completion_date": "2026-08-28", "has_results": false, "last_update_posted_date": "2026-10-01", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Stanford, California", "locations": [ { "city": "Stanford", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07706920" }, { "nct_id": "NCT07219862", "title": "Evaluating a Clinical Decision Support Tool for Antiretroviral Therapy Optimization", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV (Human Immunodeficiency Virus)", "Clinical Decision Support System (CDSS)", "Antiretroviral Therapy, Highly Active", "INDIVIDUALIZED THERAPY", "AIDS (Acquired Immune Deficiency Syndrome)", "Personalized Medicine", "Precision Medicine" ], "interventions": [ { "name": "smART (Smart Antiretroviral Therapy Assistant)", "type": "OTHER" }, { "name": "Traditional Prescribing resources", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Keck School of Medicine of USC", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2028-09-01", "completion_date": "2031-09-01", "has_results": false, "last_update_posted_date": "2025-10-22", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07219862" }, { "nct_id": "NCT05900310", "title": "Linus Health CDS Retrospective Validation Study", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cognitive Impairment", "Motor Disorders", "Dementia" ], "interventions": [ { "name": "Core Cognitive Evaluation (CCE)", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Linus Health, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "55 Years", "maximum_age": null, "sex": "ALL", "summary": "55 Years and older" }, "enrollment_count": 40, "start_date": "2023-06", "completion_date": "2023-08", "has_results": false, "last_update_posted_date": "2023-06-12", "last_synced_at": "2026-10-07T13:31:23.437Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05900310" } ] }