{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Notification+system&page=5", "query": { "intervention": "Notification system", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 118, "total_pages": 12, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Notification+system&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Notification+system&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-22T08:00:23.186Z", "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": "NCT03997331", "title": "Chronicare for Type 2 Diabetes (Chronicare-T2D)", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 2 Diabetes" ], "interventions": [ { "name": "CRx Health", "type": "OTHER" }, { "name": "Chronicare", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "QuiO", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 100, "start_date": "2020-05", "completion_date": "2021-02", "has_results": false, "last_update_posted_date": "2020-03-31", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Midland, Michigan", "locations": [ { "city": "Midland", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT03997331" }, { "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": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02726620" }, { "nct_id": "NCT04804579", "title": "Boston ARCH 4F Intervention to Reduce Fall Risk in People With HIV and Alcohol Use", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Infection", "Alcohol Consumption", "Falls, Accidental", "Falls" ], "interventions": [ { "name": "Fall Prevention Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Boston University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 23, "start_date": "2021-10-20", "completion_date": "2022-08-01", "has_results": true, "last_update_posted_date": "2023-06-29", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04804579" }, { "nct_id": "NCT06144554", "title": "Post Market Registry for the Omnipod 5 System in Children and Adults With Type 1 Diabetes", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Type 1 Diabetes" ], "interventions": [ { "name": "Omnipod 5", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Insulet Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": null, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 2200, "start_date": "2023-09-25", "completion_date": "2028-09", "has_results": false, "last_update_posted_date": "2026-07-01", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Buffalo, New York", "locations": [ { "city": "Buffalo", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06144554" }, { "nct_id": "NCT03469141", "title": "Interactive Telehealth for Pressure Ulcer Prevention After SCI", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries", "Pressure Ulcer" ], "interventions": [ { "name": "Pressure Relief Monitoring System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Rancho Research Institute, Inc.", "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": 100, "start_date": "2018-05-01", "completion_date": "2021-10-30", "has_results": false, "last_update_posted_date": "2018-06-13", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 4, "location_summary": "Birmingham, Alabama • Downey, California • Miami, Florida + 1 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Downey", "state": "California" }, { "city": "Miami", "state": "Florida" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03469141" }, { "nct_id": "NCT01255865", "title": "Comparison Study of Core Temperature Thermometry Systems", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Thermometry Device Comparisons" ], "interventions": [], "intervention_types": [], "sponsor": "3M", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 111, "start_date": "2010-12", "completion_date": "2011-12", "has_results": true, "last_update_posted_date": "2020-08-25", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01255865" }, { "nct_id": "NCT01346839", "title": "Effectiveness of Electronic Health Record-Based Interventions for Improving Follow-Up in Primary Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colon Cancer", "Lung Cancer", "Prostate Cancer" ], "interventions": [ { "name": "Contact Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Baylor College of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 1256, "start_date": "2011-02", "completion_date": "2012-08", "has_results": true, "last_update_posted_date": "2016-02-09", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 2, "location_summary": "Houston, Texas • Temple, Texas", "locations": [ { "city": "Houston", "state": "Texas" }, { "city": "Temple", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01346839" }, { "nct_id": "NCT02274688", "title": "A Comparative Effectiveness Trial of Optimal Patient-Centered Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post Traumatic Concerns", "Post Traumatic Stress Disorder", "Depression and Suicide Ideation", "Alcohol and Drug Use" ], "interventions": [ { "name": "Stepped Care Management", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": null, "sex": "ALL", "summary": "14 Years and older" }, "enrollment_count": 171, "start_date": "2014-03", "completion_date": "2016-12-31", "has_results": true, "last_update_posted_date": "2017-11-21", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT02274688" }, { "nct_id": "NCT05733767", "title": "Smoking Cessation Pharmacotherapy-Nurse Practitioner Led Tobacco Treatment Team Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Cardiopulmonary Disease", "Smoking Cessation", "Inpatient" ], "interventions": [ { "name": "Enhanced Usual Care (EUC)", "type": "OTHER" }, { "name": "Nurse Practitioner Tobacco Treatment Team (NPT3)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Baystate 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": 424, "start_date": "2022-11-03", "completion_date": "2027-12-30", "has_results": false, "last_update_posted_date": "2026-10-01", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Springfield, Massachusetts", "locations": [ { "city": "Springfield", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT05733767" }, { "nct_id": "NCT04556240", "title": "RECORD-VP: Real-time Evaluation of Cardiac Outpatient Recording Device With VitalPatch RTM", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Arrhythmias, Cardiac" ], "interventions": [ { "name": "VitalConnect Platform", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "VitalConnect Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2020-09-15", "completion_date": "2020-11-30", "has_results": false, "last_update_posted_date": "2023-07-27", "last_synced_at": "2026-10-22T08:00:23.186Z", "location_count": 1, "location_summary": "Chevy Chase, Maryland", "locations": [ { "city": "Chevy Chase", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT04556240" } ] }