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RECRUITING
NCT04504188
NA

Optimizing Beta Blocker Dosage in Women While Using the Wearable Cardioverter Defibrillator

Sponsor: Zoll Medical Corporation

View on ClinicalTrials.gov

Summary

The primary objective of this pilot study is to document the percentage achievement in effective HR control (average nighttime HR \< 70 bpm) during WCD use in a cohort of female patients with cardiomyopathy in an outpatient setting using continuous heart rate (HR) trends data from the WCD to optimize BB/ivabradine dosage, as compared to a prior historical control.

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

300

Start Date

2021-03-08

Completion Date

2024-12

Last Updated

2024-07-24

Healthy Volunteers

No

Interventions

DEVICE

Heart Rate Monitor Enhanced Treatment Optimization

Heart rate (HR) will be continuously monitored by the WCD. Every two weeks a report showing daily HR trends will be emailed to the healthcare provider. The healthcare provider will also receive a HR control alert if the HR exceeds a predetermined threshold for 3 days in a row.

Locations (4)

TriHealth Hatton Research Institute

Cincinnati, Ohio, United States

Texas Cardiology Associates of Houston

Kingwood, Texas, United States

CardioVoyage

McKinney, Texas, United States

CAMC

Charleston, West Virginia, United States