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CompletedNCT00205257Updated Oct 5, 2015

Prediction of Acute Rejection in Renal Transplant

An observational study in Kidney Transplant, sponsored by University of Wisconsin, Madison. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-10-05.

Sponsored by University of Wisconsin, Madison · Observational

Study type
Observational
Ages
18 Years and older
Sex
All
01

Study summary

Acute rejection is still a major risk factor affecting the prognosis of kidney transplant patients. Alloreactive cells of the recipient infiltrate the kidney graft and cause inflammatory reaction which damages the graft structure and function. Conventional diagnosis of acute rejection is based on clinical symptoms and kidney biopsy examination. The clinical symptoms are a result of the kidney damage, which occurs days after the initiation of the rejection reaction. Kidney biopsy is an invasive and expensive procedure. It has been wished to have new parameters that can replace/supplement the conventional procedures. Chemokines are small molecules that attract inflammatory cells. Changes of chemokine levels in the urine may correlate with the immune status in the kidney. A systematic study to evaluate the chemokine levels in urine and correlation with the kidney biopsy pathology will answer the question whether monitoring of urinary chemokines would be useful in predicting graft rejection/damage.

02

Conditions studied

  • Kidney Transplant
03

In context

Lead sponsor

University of Wisconsin, Madison is the lead sponsor of 1,161 studies on the registry; 182 are open to participants now.

Of its 151 completed or terminated interventional studies of FDA-regulated products, 114 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • One hundred subjects undergoing kidney biopsy for suspected rejection
  • Forty subjects that have stable graft function with normal level of blood creatinine (No biopsy is needed at the time of sample collection).

Exclusion criteria

Exclusion Criteria:

  • Subjects under the age of 18
  • Gender of potential subjects male or female
  • Age Limits greater than 18 years of age
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Study design

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What researchers measure

Primary outcomes

  1. kidney biopsy pathology

    Time frame: 1 year

Secondary outcomes

  1. urinary chemokines

    Time frame: 1 year

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 5, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00205257
Lead sponsor
University of Wisconsin, Madison
Responsible party
Sponsor
First posted
Sep 20, 2005
Start date
Sep 2001
Primary completion
Feb 2007
Completion
Feb 2007
Last update
Oct 5, 2015

Study contacts

Thomas Chin
principal investigator · University of Wisconsin Medical School
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2013. You cannot join it, but the record below documents what was studied.

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