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By physician referral or invitation only

Heartcare Outcomes Registry

The purpose of this registry is to observe outcomes of heart transplant recipients who are managed with HeartCare. This is done by collecting information about your heart transplant such as test results, biopsy results, and outcomes, storing that information in a database, and using that information for research.

Age & Gender

  • 21 years ~ 99 years
  • Male, Female

Contact the Team

Location

Thank you for your interest, but this study is recruiting by invitation only.

North Carolina (Statewide)

Additional Study Information

Principal Investigator

Patricia Chang
Medicine - Cardiology

Study Type

Clinical or Medical
Registry

Study Topics

Transplant

IRB Number

19-2694

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