[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"heart-failure-with-reduced-ejection-fraction-hypertension\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:heart-failure-with-reduced-ejection-fraction-hypertension":39},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":25,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":5},"100640140",false,"NCT07626879","Feasibility and Effectiveness of a Ring-Type Blood Pressure Device (CART-BP) Compared With 24-Hour Ambulatory Blood Pressure Monitoring in HFrEF","Feasibility and Effectiveness of a RING-type Blood Pressure Measurement Device (CART-BP) Compared With 24-Hour Ambulatory Blood Pressure Monitoring Device in Patients With Heart Failure With Reduced Ejection Fraction (RING-HFrEF)","RING-HFrEF","Inclusion Criteria:\n\n1. Age ≥ 19 years (male or female)\n2. Diagnosed with heart failure and currently under treatment\n3. Left ventricular ejection fraction (LVEF) ≤ 40% confirmed by echocardiography performed within 1 year prior to enrollment\n4. Able to undergo both 24-hour ambulatory blood pressure monitoring and ring-type blood pressure measurement\n5. Voluntarily provided written informed consent to participate in this clinical study\n\nExclusion Criteria:\n\n1. Office blood pressure: SBP \\\u003C 90 mmHg, or DBP \\\u003C 50 mmHg, or SBP \\> 180 mmHg, or DBP \\> 100 mmHg\n2. Unable to perform 24-hour ambulatory blood pressure monitoring\n3. Unable to wear or use the ring-type blood pressure device\n4. Variability in three consecutive resting cuff blood pressure measurements ≥ 20 mmHg (SBP) or ≥ 10 mmHg (DBP)\n5. Insufficient valid ABPM readings: \\\u003C 25 daytime or \\\u003C 12 nighttime measurements per ESH criteria; or \\\u003C 25 daytime or \\\u003C 12 nighttime valid readings from the ring-type device\n6. Pregnant, suspected pregnancy, or breastfeeding\n7. Judged by the investigator to be legally or mentally unfit to participate in the clinical study","ALL","19 Years",{"count":19,"type":20},100,"ESTIMATED","OBSERVATIONAL","This study aims to evaluate the feasibility and diagnostic accuracy of the CART-BP ring-type wearable blood pressure monitoring device in comparison with 24-hour ambulatory blood pressure monitoring (ABPM) in patients with heart failure with reduced ejection fraction (HFrEF, LVEF ≤ 40%). As a multi-center, prospective, exploratory study, 100 patients will be enrolled at two tertiary hospitals in South Korea. The agreement between the two devices in 24-hour mean, daytime, and nighttime blood pressure measurements will be assessed per ISO 81060-2:2018 criteria.",[24],"Heart Failure With Reduced Ejection Fraction; Hypertension",[26],"HFrEF, ambulatory blood pressure monitoring, ABPM, wearable device, ring-type blood pressure, photoplethysmography, PPG, blood pressure validation","RECRUITING","2026-05-29",{"date":30,"type":31},"2026-06-04","ACTUAL",{"date":33,"type":31},"2025-10-23",{"date":35,"type":20},"2026-10-22",{"name":37,"class":38},"Keimyung University Dongsan Medical Center","OTHER",""]