Skip to main content
Clinical Trials/NCT01331668
NCT01331668
Recruiting
Not Applicable

Biobank Renal Transplantation University Hospitals Leuven

Universitaire Ziekenhuizen KU Leuven1 site in 1 country5,000 target enrollmentStarted: March 2004Last updated:
ConditionsKidney Failure

Overview

Phase
Not Applicable
Status
Recruiting
Enrollment
5,000
Locations
1
Primary Endpoint
Renal allograft survival

Overview

Brief Summary

This study aims to maintain a prospective biobank of human samples obtained from donors and recipients of renal allografts, including biopsy tissue, peripheral blood samples and urine samples.

Detailed Description

Clinical data and bio-specimens are prospectively collected and stored for undefined future translational research projects.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • renal transplant recipients/donors

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Renal allograft survival

Time Frame: 50 years after transplantation

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Prof Dr Maarten Naesens

Prof. Dr. Maarten Naesens

Universitaire Ziekenhuizen KU Leuven

Study Sites (1)

Loading locations...

Similar Trials