BIOBANK Renal Transplantation University Hospitals Leuven

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.

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Key information

Conditions

Kidney Failure Female Urogenital Diseases Female Urogenital Diseases and Pregnancy Complications Kidney Diseases Male Urogenital Diseases Renal Insufficiency Urogenital Diseases Urologic Diseases

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Nephrology and Renal Transplantation - University Hospitals Leuven

Leuven, BE, 3000, Belgium

Location status: Recruiting

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

renal transplant recipients/donors

Exclusion criteria

none

Treatment and study plan

Primary outcomes

Renal allograft survival

Time frame: 50 years after transplantation

Interested in participating?

Recruiting

Interested in participating?

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Sponsors and collaborators

Lead sponsor

Universitaire Ziekenhuizen KU Leuven

Other

Registry information

Important dates

Study start: 2004
Primary completion: 2099
Study completion: 2099
First posted: Apr 8, 2011
Registry last updated: May 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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