The Use of CoSeal (Sealant Agent) in Patients During Left Ventricular Assist Device Surgery

This study has been terminated.
(funding for study stopped)
Sponsor:
Information provided by (Responsible Party):
Brian A. Bruckner, M.D., The Methodist Hospital System
ClinicalTrials.gov Identifier:
NCT01605019
First received: May 21, 2012
Last updated: April 6, 2015
Last verified: April 2015
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study has been terminated.
  Study Completion Date: March 2014
  Primary Completion Date: March 2014 (Final data collection date for primary outcome measure)