Accuracy of Cardiac Acoustic Biomarkers Recorded by the Wearable Cardioverter Defibrillator
NCT04292405 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 60
Last updated 2025-10-30
Summary
Evaluate data accuracy of cardiac acoustic biomarkers (CABs) recorded by the Wearable Cardioverter Defibrillator (WCD) as compared to the AUDICOR AM acoustic cardiography recorder.
Conditions
Interventions
- DEVICE
-
Wearable Cardioverter Defibrillator
Use of the Wearable Cardioverter Defibrillator and AUDICOR AM to evaluate accuracy of cardiac acoustic biomarker recordings.
Sponsors & Collaborators
-
Zoll Medical Corporation
lead INDUSTRY
Principal Investigators
-
Mike Osz · Director, Clinical Operations, ZOLL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-01-23
- Primary Completion
- 2025-09-30
- Completion
- 2025-09-30
- FDA Device
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Cardiac Resynchronization Therapy Defibrillator Based Impedance Monitoring Study
NCT00500838 ·Status: COMPLETED ·Phase: NA
-
Cardiac Resynchronization Therapy (CRT)-Narrow-dp/Dt-Study
NCT00821938 ·Status: COMPLETED ·Phase: PHASE4
-
Catheter Ablation Versus Amiodarone for Shock Prophylaxis in Defibrillator Patients With Ventricular Tachycardia
NCT01097330 ·Status: TERMINATED ·Phase: PHASE3
-
Human Use Condition Study- Evaluation of Implanted Leads in Humans
NCT04320849 ·Status: COMPLETED
-
Myocardial Injury in Patients With Cardiac Implantable Electronic Devices Undergoing Defibrillation Threshold Testing
NCT04284800 ·Status: ACTIVE_NOT_RECRUITING
-
Safety and Efficacy of Automatic Testing Feature in New ICDs and CRT-Ds
NCT00746356 ·Status: COMPLETED ·Phase: NA
-
Resynchronization/Defibrillation for Ambulatory Heart Failure Trial
NCT00251251 ·Status: COMPLETED ·Phase: NA
-
Reduction of Inappropriate Shocks of Implantable Cardioverter Defibrillators (ICDs) With Enhanced SVT Discriminators
NCT01963286 ·Status: COMPLETED ·Phase: NA
-
Heart Sounds Registry
NCT03203629 ·Status: COMPLETED
-
Empiric Versus Imaging Guided Left Ventricular Lead Placement in Cardiac Resynchronization Therapy
NCT01323686 ·Status: COMPLETED ·Phase: NA
-
Ensure Cardiac Resynchronization Therapy Study
NCT00291564 ·Status: COMPLETED
-
The Ability Of The PD2i Cardiac Analyzer To Predict Risk Of Ventricular Tachyarrhythmic Events
NCT00510731 ·Status: WITHDRAWN
-
MAgnetic Resonance Imaging-guided implanTation of Cardioverter DEFibrillators
NCT06269692 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Acute Feedback on Left ventrIcular Lead Implantation Location for Cardiac Resynchronization Therapy
NCT01996397 ·Status: COMPLETED ·Phase: NA
-
MASTER I - Microvolt T Wave Alternans Testing for Risk Stratification of Post MI Patients
NCT00305240 ·Status: COMPLETED ·Phase: NA
-
Trial in Cardiac Resynchronization Therapy (CRT): Right Ventricular Apex Versus High Posterior Septum
NCT01035489 ·Status: UNKNOWN ·Phase: PHASE2
-
Efficacy of Implantable Cardioverter Defibrillator in Patients With Non-ischemic Systolic Heart Failure on Mortality
NCT00541268 ·Status: COMPLETED ·Phase: NA
-
Circulating Biomarkers and Ventricular Tachyarrhythmia
NCT01892462 ·Status: COMPLETED
-
Optimizing Beta Blocker Dosage in Women While Using the Wearable Cardioverter Defibrillator
NCT04504188 ·Status: RECRUITING ·Phase: NA
-
MyoVista wavECG Clinical Validation Study Versus Low e' on Echocardiogram
NCT04804969 ·Status: UNKNOWN
-
Comparison of Right Ventricular Septal and Right Ventricular Apical Pacing in Patients Receiving a CRT-D Device
NCT00833352 ·Status: COMPLETED ·Phase: NA
-
Efficacy of the ATP Switch Automatic Programming in Implantable Cardioverter Defibrillator (ICD) and Cardiac Resynchronization Therapy Defibrillator (CRT-D) Implanted Patients
NCT01169246 ·Status: TERMINATED
-
Validation of CardioMEMS HF System Cardiac Output Algorithm IDE
NCT05428384 ·Status: COMPLETED
-
Myocardial Injury Following Elective Direct Current Cardioversion for Atrial Arrhythmias
NCT04151966 ·Status: COMPLETED
-
Magnetic Resonance (MR) Conditional Tachyarrhythmia Therapy Products Post-approval Study
NCT02849769 ·Status: COMPLETED