Personalized Therapy Study - HFRS (TriageHF) Post Approval Study

Status Recruiting

Clinical Trial Summary

Medtronic is sponsoring the HFRS PAS to evaluate the HFRS feature (TriageHF) when used in routine clinical practice following commercial release. The HFRS PAS is conducted within Medtronic's Product Surveillance Registry (PSR) platform.

Clinical Trial Description

The HFRS PAS is a global, prospective, observational, multi-site study. Patients implanted with a Medtronic Cobalt™ XT CRT (with Attain StabilityQuad™ MRI SureScan™ Model 4798 Lead (ASQ)) or ICD device who are enrolled in the Medtronic CareLink (CL) Network and the PSR will be followed per the standard of care practices of their care provider. ;

Study Design

Related Conditions & MeSH terms

Heart Failure

Clinical Trial Details

NCT number	NCT04489225
Study type	Observational
Source	Medtronic
Contact	PSR Study Team
Phone	1-800-633-8766
Email	rs.productsurveillanceregistry@medtronic.com
Status	Recruiting
Phase
Start date	August 1, 2020
Completion date	January 31, 2027

View Details

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