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Cardiac Resynchronization Therapy (CRT) Based Heart Failure Monitoring Study


CRT-D Based Heart Failure Monitoring Study




The purpose of this study is to collect and analyze electrical measurements, timing, and signals from a CRT-D device in heart failure patients who either already have an implanted left atrial pressure sensor or will undergo a simultaneous implantation of a left atrial pressure sensor and a CRT-D device. These devices may be placed at the same time or separately (staged procedure) at the discretion of the investigator. A comparison will be made between the information gathered from the CRT-D system and the information gathered by the left atrial pressure sensor.

Study Status: Active, not recruiting


Condition Intervention Phase
Heart Failure Device: Cardiac resynchronization therapy and HeartPODĀ® system Phase 2

Verified by St. Jude Medical December, 2012

Sponsored by: St. Jude Medical
Information provided by: St. Jude Medical identifier: NCT00632372

Study Type: Interventional

Study Design: Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

The Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States

Richard Troughton, MD., Principal Investigator

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