Recruitment

Recruitment Status
Recruiting
Estimated Enrollment
90

Summary

Conditions
Congestive Heart Failure
Type
Observational
Design
Observational Model: CohortTime Perspective: Prospective

Participation Requirements

Age
Between 13 years and 125 years
Gender
Both males and females

Description

Brief description of procedures: After informed consent is obtained from the patient, the blood samples will be obtained either during a procedure from access lines inserted for the procedure or they will be drawn when other ordered lab work is done at specific time points during the study. Tissue s...

Brief description of procedures: After informed consent is obtained from the patient, the blood samples will be obtained either during a procedure from access lines inserted for the procedure or they will be drawn when other ordered lab work is done at specific time points during the study. Tissue samples will be obtained at the time of LVAD implantation by keeping the part of the left ventricular apex that the surgeon is removing in order to place the inflow cannula of the LVAD. No extra tissue sample, other than the tissue that has to be removed as a part of a standard LVAD, will be collected.

Tracking Information

NCT #
NCT01099982
Collaborators
  • Intermountain Health Care, Inc.
  • VA Salt Lake City Health Care System
  • Hunter Holmes McGuire VA Medical Center
Investigators
Study Director: Dean Y Li, M.D., Ph.D. University of Utah Principal Investigator: Josef Stehlik, M.D., M.P.H. University of Utah Health Sciences Center & VA Salt Lake City Health Care System Study Director: Stavros G Drakos, M.D., Ph.D. University of Utah