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Confirmation Trial of the Acorn CorCap Cardiac Support Device (CSD) at the Same Time as Mitral Valve Repair

Study:

Clinical Evaluation of Acorn CorCap Cardiac Support Device Concomitant to MVR - A Confirmatory Trial

Rationale:

n/a

Purpose:

The purpose of this study to evaluate patients when they have an Acorn CorCapTM Cardiac Support Device (CSD) placed around their heart for the treatment of heart failure at the same time as their mitral valve surgery. The CorCapTM CSD is intended to support the heart, potentially preventing further dilation that is associated with progressive heart failure, thereby potentially preserving or improving heart function.

Study Status: Recruiting

Recruiting:
Barb Gus, RN 216-445-6552 gusb@ccf.org

Condition Intervention Phase
Heart Failure Device: CorCap CSD Phase 2

Verified by Acorn Cardiovascular, Inc. June, 2009

Sponsored by: Acorn Cardiovascular, Inc.
Information provided by: Acorn Cardiovascular, Inc.
ClinicalTrials.gov identifier: NCT00630266

Study Type: Interventional

Study Design: Supportive Care, Non-Randomized, Open Label, Single Group Assignment, Safety/Efficacy Study

Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States

Steven F Bolling, MD., Principal Investigator
Michael A Acker, MD., Principal Investigator
Mario Pompili, MD., Principal Investigator
James Wudel, MD., Principal Investigator
Randall Starling, MD., Principal Investigator
Mark J Zucker, MD, JD., Principal Investigator
Renzo Cecere, MD., Principal Investigator
Pat Pappas, MD., Principal Investigator
Robert Brewer, MD., Principal Investigator
Jeff Cope, MD., Principal Investigator
Edward Raines, MD., Principal Investigator

This information is abridged to display results relevant only to Cleveland Clinic. To see complete record visit ClinicalTrials.gov
  Information obtained from ClinicalTrials.gov on
Link to the current ClinicalTrials.gov record.

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