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Safety and Performance of Electrodes Implanted in the Left Ventricle — SELECT-LV  

Heart Failure Clinical Trial

Official title:
Multicenter, Prospective Evaluation of Safety and Performance of the WiCS-LV System in Patients Indicated for Cardiac Resynchronization Therapy

Clinical Trial Summary

The study is intended to demonstrate the safe implant of small receiver-electrodes into the endocardial surface of the left ventricle and to demonstrate its utility in providing cardiac resynchronization therapy in heart failure patients.

Clinical Trial Description

Eligible patients will undergo an acoustic window assessment using transthoracic echocardiography. Patients with adequate acoustic windows will undergo implantation of the WiCS-LV system.

Patients will undergo evaluations pre-hospital discharge, and at one month, 3 months, and 6 months post implantation. Extended follow-up will be obtained via a registry at 1, 2, 3, 4, and 5 years post implantation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01905670
Study type Interventional
Source EBR Systems, Inc.
Contact
Status Completed
Phase N/A
Start date July 2013
Completion date November 2019
View Details
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