Identification of Genomic Predictors of Adverse Events After Cardiac Surgery

Status: Recruiting
Location: See all (3) locations...
Study Type: Observational
SUMMARY

This study aims to identify genetic causes of adverse events after cardiac surgery, such as atrial fibrillation, myocardial infarction, renal dysfunction and heart failure. Patients undergoing heart surgery at Brigham and Women's Hospital and Texas Heart Institute are eligible to participate.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 20
Maximum Age: 90
Healthy Volunteers: f
View:

• Undergoing heart surgery

• Willing to provide consent

Locations
United States
Massachusetts
Brigham and Women's Hospital
COMPLETED
Boston
Texas
UT Southwestern Medical Center
RECRUITING
Dallas
Department Texas Heart Institute at St. Luke's Episcopal Hospital
COMPLETED
Houston
Time Frame
Start Date: 2000-08
Estimated Completion Date: 2030-08
Participants
Target number of participants: 4000
Treatments
Cardiac surgery
Adult patients undergoing cardiac surgery
Sponsors
Leads: Brigham and Women's Hospital
Collaborators: Texas Heart Institute, Johns Hopkins University, National Heart, Lung, and Blood Institute (NHLBI), University of Texas Southwestern Medical Center

This content was sourced from clinicaltrials.gov