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Studies genes linked to problems after heart surgery

Looks for genetic causes of complications, such as atrial fibrillation, after heart surgery.

Plain-language title generated from the registry record
Registry title: Identification of Genomic Predictors of Adverse Events After Cardiac Surgery

Key facts

Where
Boston, Dallas, and Houston, United StatesSee the 3 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 20 and 90 years old?

Source: NCT01258231, who can take part

Where in United States

  • Brigham and Women's HospitalBoston, United StatesNo longer taking part
  • UT Southwestern Medical CenterDallas, United StatesTaking people
  • Department Texas Heart Institute at St. Luke's Episcopal HospitalHouston, United StatesNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
Brigham and Women's Hospital
Trial code
NCT01258231
Record updated
22 August 2024
Original 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.Read full original descriptionShow less

Identification of Genomic Predictors of Adverse Events After Cardiac Surgery

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.

Inclusion: Undergoing heart surgery; Willing to provide consent.

Exclusion: Enrolled in a concurrent drug or device trial that precludes concurrent enrollment.

ClinicalTrials.gov NCT01258231