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Recruiting NCT01094327

Proteinuria in Pre and Post Transplant

Observational Proteinuria

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Proteinuria. Basic parameters: up to 25 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Evaluation of Recipients With and Without Proteinuria, Pre and Post Kidney Transplantation

Overview

Patients with focal segmental glomerulosclerosis (FSGS) who progress rapidly to end stage renal disease (ESRD) are at highest risk for development of recurrence of proteinuria following kidney transplantation. This study will look at serum specimens pre and post transplant, as well as kidney transplant specimens pre and post reperfusion to identify where the defects has occured that results in recurrence of proteinuria in a given kidney transplant.

Detailed description

This study will retrospectively review patient's medical records for protein in the urine, blood creatinine and kidney biopsy results. Also character of the fluid used to flush the kidney before transplant will be analyzed.

Primary outcome measures

  • Explain mechanisms behind the development of proteinuria in patients immediately after receiving a kidney transplant [Time frame: through study completion, an average of 5 years]

Eligibility criteria

Inclusion criteria

  • Kidney transplant recipients
  • Pediatric males and females up to the age of 25 years old.

Exclusion criteria

  • Transplant recipients other than kidney

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

United States · 1 center
  • University of Miami Miller School of Medicine Transplant Clinic — Miami

Identifiers

NCT: NCT01094327 · 20070206

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗