Kidney Transplantation Clinical Trial
Official title:
Noninvasive Diagnosis of Renal Allograft Rejection by Urinary Cell mRNA Profiling
The purpose of this study is to determine if analysis of urine samples for specific markers can predict transplant rejection in people who have received kidney transplants.
Innovations in kidney transplantation have improved short-term outcomes for transplant
patients. However, organ rejection remains as an important threat to the long-term survival
of the transplanted organ. An increase in the serum creatinine level is often the first
clinical indicator of kidney transplant rejection; however, this marker lacks sensitivity
and specificity. Rejection is currently diagnosed using an invasive transplant biopsy
procedure; in addition to being expensive, transplant biopsies can result in bleeding from
the transplant and even graft loss. In early studies, it has been observed that significant
increases in the levels of perforin, granzyme B, and CD3 messenger RNA (mRNA) in urinary
cells signal the development of acute transplant rejection. The purpose of this study is to
evaluate whether the noninvasive procedure of measuring perforin, granzyme B, and CD3 mRNA
levels in urine samples can accurately diagnose and predict kidney transplant rejection,
make transplant biopsy unnecessary, and provide an opportunity to initiate treatment for
early rejection with the aim to minimize damage to the kidney.
This study will last 3 years post-transplant. There will be a total of 14 study visits.
Blood and urine collection will occur at all visits. Additional visits may be necessary for
those participants who develop abnormal kidney function.
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Observational Model: Cohort, Time Perspective: Prospective
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