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Clinical Trial Summary

This is a prospective, multicenter, non-randomized registry/observational study. The study will enroll up to 200 patients with successful St. Jude Medical (SJM) Cardiac Resynchronization Therapy (CRT) MP device implant from up to 10 centers.

Clinical Trial Description

Any patient receiving a market-approved SJM Quadra Assura MP (CRT-D) or newer model quadripolar device with MPP capability and who meets the inclusion criteria and none of the exclusion criteria is eligible for enrollment in the study.

Patients will be followed for 12 months after implant. Data will be collected after device implant (up to 30 days after successful implant), at 3, 6 and 12 months post-implant and during unscheduled visits. ;

Study Design

Related Conditions & MeSH terms

NCT number NCT03001141
Study type Observational [Patient Registry]
Source Abbott Medical Devices
Status Terminated
Start date May 18, 2017
Completion date February 8, 2019