Urine Testing to Detect Kidney Transplant Rejection
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Purpose
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.
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Noninvasive Diagnosis of Renal Allograft Rejection by Urinary Cell mRNA Profiling |
Blood and urine collection
| Enrollment: | 492 |
| Study Start Date: | June 2006 |
| Study Completion Date: | December 2010 |
| Primary Completion Date: | December 2010 (Final data collection date for primary outcome measure) |
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.
Eligibility| Ages Eligible for Study: | up to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Patients who have recently undergone kidney transplant
Inclusion Criteria:
- Scheduled to undergo primary or redo deceased- or living-donor kidney transplantation
- Ability to provide informed consent
Exclusion Criteria:
- Requires combined organ transplantation
- Previously received a solid organ transplant (other than kidney transplant) or islet cell transplant
- HCV infected
- HIV infected
Contacts and Locations| United States, Illinois | |
| Northwestern University | |
| Chicago, Illinois, United States, 60611 | |
| United States, New York | |
| Columbia University | |
| New York, New York, United States, 10032 | |
| Cornell University | |
| New York, New York, United States, 10021 | |
| United States, Pennsylvania | |
| University of Pennsylvania | |
| Philadelphia, Pennsylvania, United States, 19104 | |
| United States, Wisconsin | |
| University of Wisconsin | |
| Madison, Wisconsin, United States, 53792 | |
| Study Chair: | Abraham Shaked, MD, PhD | Department of Surgery, University of Pennsylvania Medical Center |
| Principal Investigator: | John Friedewald, MD | Northwestern University |
| Principal Investigator: | Stuart Knechtle, MD | Department of Surgery, University of Wisconsin |
| Principal Investigator: | Jean Emond, MD | Department of Surgery, Columbia University |
| Principal Investigator: | Darshana Dadhania, MD | Cornell University |
More Information
Additional Information:
Publications:
| Responsible Party: | National Institute of Allergy and Infectious Diseases (NIAID) |
| ClinicalTrials.gov Identifier: | NCT00337220 History of Changes |
| Other Study ID Numbers: | DAIT CTOT-04 |
| Study First Received: | June 14, 2006 |
| Last Updated: | February 6, 2013 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
|
allograft graft |
Additional relevant MeSH terms:
|
Kidney Diseases Kidney Failure, Chronic Renal Insufficiency Urologic Diseases Renal Insufficiency, Chronic |
ClinicalTrials.gov processed this record on June 18, 2013