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Integrated Diagnostics Driven Diuretic and Chronic Medication Management for Heart Failure

Heart Failure Clinical Trial

Official title:
Integrated Diagnostics Driven Diuretic and Chronic Medication Management for Heart Failure

Clinical Trial Summary

The INTERVENE-HF study is a prospective, non-randomized, multi-center (US only), investigational, feasibility study. The purpose of this study is to characterize safety of managing heart failure patients with integrated device diagnostics that have an implanted commercially available Medtronic cardiac resynchronization therapy defibrillator (CRT-D).

Clinical Trial Description

The study is expected to be conducted at up to 20 centers located in the United States. Up to 400 subjects will be enrolled to yield up to 200 eligible subjects that meet screening criteria. This study will be conducted in subjects with an implanted, commercially available, Medtronic, CRT-D device. Each enrolled subject will be followed every 2 months from time of enrollment to end of the study.The study will end after the last enrolled subject completes the 12-month follow-up. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02698241
Study type Interventional
Source Medtronic Cardiac Rhythm and Heart Failure
Contact
Status Terminated
Phase N/A
Start date May 2016
Completion date September 2018
View Details
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