Clinical Trials Directory

Trials / Recruiting

RecruitingNCT01258231

Identification of Genomic Predictors of Adverse Events After Cardiac Surgery

Status
Recruiting
Phase
Study type
Observational
Enrollment
4,000 (estimated)
Sponsor
Brigham and Women's Hospital · Academic / Other
Sex
All
Age
20 Years – 90 Years
Healthy volunteers
Not accepted

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.

Detailed description

This study aims to identify genetic causes of adverse events after cardiac surgery, such as atrial fibrillation, myocardial infarction, renal dysfunction and heart failure. In addition, we also examine blood and urine biomarkers (proteins).

Conditions

Timeline

Start date
2000-08-01
Primary completion
2030-08-01
Completion
2030-08-01
First posted
2010-12-10
Last updated
2024-08-22

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01258231. Inclusion in this directory is not an endorsement.

Identification of Genomic Predictors of Adverse Events After Cardiac Surgery (NCT01258231) · Clinical Trials Directory