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RECRUITING
NCT06570902

Prospective WCD Post CABG Registry (CABG Registry)

Sponsor: Zoll Medical Corporation

View on ClinicalTrials.gov

Summary

The primary objective is to observe the rate of recovery of ventricular function (EF\>35%) after first-time coronary artery bypass graft surgery in patients who were prescribed the wearable cardioverter defibrillator (WCD) post-surgery prior to being discharged after hospitalization as part of standard clinical care.

Official title: Prospective WCD Post CABG Registry

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

910

Start Date

2024-09-23

Completion Date

2030-05

Last Updated

2024-11-04

Healthy Volunteers

Not specified

Interventions

DEVICE

WCD

An FDA-approved, CE marked WCD will be prescribed for up to 3 months of use after hospital discharge, with the option for longer use under physician discretion

Locations (4)

Kerckhoff Klinik

Bad Nauheim, Hesse, Germany

Medizinische Hochschule Hannover

Hanover, Lower Saxony, Germany

Sana-Herzzentrum Cottbus GmbH

Cottbus, Germany

Universitätsklinikum Halle (Saale)

Halle, Germany