Last updated on September 2018

The Product Surveillance Registry REVERSE Post Approval Study


Brief description of study

The purpose of the REVERSE Post Approval Study (PAS) is to confirm the benefit observed in the REVERSE and RAFT pivotal studies in "real-world" clinical practice.

Detailed Study Description

The REVERSE PAS will estimate the 3-year survival probability of freedom from heart failure hospitalization and heart failure events in patients implanted with a Medtronic CRT-D device who meet the expanded indication criteria with a QRS duration 150 ms.

Clinical Study Identifier: NCT01660035

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Medtronic Product Surveillance Registry

Colorado Springs, CO United States
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Medtronic Product Surveillance Registry

West Des Moines, IA United States
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Medtronic Product Surveillance Registry

Saint Louis Park, MN United States
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Medtronic Product Surveillance Registry

Charlottesville, VA United States
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Recruitment Status: Open


Brief Description Eligibility Contact Research Team


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