TruGraf® Long-term Clinical Outcomes Study

Overview

About this study

The purpose of this study is to evaluate post-transplant clinical outcomes in receipients of kidney transplants who are undergoing TruGraf® and TRAC™ monitoring.

 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Written informed consent and HIPAA authorization.
  • At least 18 years of age.
  • Recipient of a primary or subsequent deceased-donor or living-donor kidney transplant.
  • At least 1-year post-transplant (+/- 2 months).
  • Stable serum creatinine (current serum creatinine < 2.3 mg/dl, < 20% increase compared to the average of the previous 3 serum creatinine levels).
  • Treated with any immunosuppressive regimen.
  • Selected by provider to undergo TruGraf® and TRAC™ testing as part of post-transplant care.
  • Has Medicare Part B coverage or private insurance

Exclusion Criteria:

  • Recipient of a combined organ transplant with an extra-renal organ and/or islet cell transplant.
  • Recipient of a previous non-renal solid organ and/or islet cell transplant.
  • Known to be pregnant.
  • Known to be infected with Human Immunodeficiency Virus (HIV).
  • Known to have BK nephropathy.
  • Known to have nephrotic proteinuria (urine protein > 3 gm/day).

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status

Scottsdale/Phoenix, Ariz.

Mayo Clinic principal investigator

Hasan Khamash, M.D.

Closed for enrollment

More information

Publications

Publications are currently not available
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CLS-20517832

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