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Wearable Cardioverter Defibrillator in Hemodialysis Patients (WED-HED) Study — WED-HED  

Sudden Cardiac Death Clinical Trial

Official title:
Wearable Cardioverter Defibrillator in Hemodialysis Patients (WED-HED) Study

Clinical Trial Summary

A multi-center, prospective, randomized controlled clinical trial with 1:1 assignment of treatment and control. This study will evaluate the impact of wearable cardioverter defibrillator use on sudden cardiac death in incident hemodialysis patients. The study will enroll up to 2,600 subjects. A maximum of 200 sites in the USA will be used for enrollment.

Clinical Trial Description

Objective: To study the impact of wearable cardioverter defibrillator (WCD) use on sudden cardiac death in hemodialysis patients. Study Population: Participants will be patients beginning hemodialysis (<2 months from initiation) who are ≥ 50 years old. Intervention: A WCD will be used for protection against sudden cardiac death (SCD). Study Design: The study will be a multi-center, prospective, randomized controlled trial with 1:1 assignment of treatment and control. Study Size: The study will enroll up to 2,600 subjects. A maximum of 200 sites will be used for enrollment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02481206
Study type Interventional
Source Zoll Medical Corporation
Contact
Status Terminated
Phase N/A
Start date June 2015
Completion date December 2017
View Details
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