Biobank for kidney transplant donors and recipients
Biobank Renal Transplantation University Hospitals Leuven
Universitaire Ziekenhuizen KU Leuven · NCT01331668
This study is setting up a collection of samples from kidney transplant donors and recipients to help researchers find ways to improve kidney transplant outcomes in the future.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 5000 (estimated) |
| Sex | All |
| Sponsor | Universitaire Ziekenhuizen KU Leuven (other) |
| Locations | 1 site (Leuven, BE) |
| Trial ID | NCT01331668 on ClinicalTrials.gov |
What this trial studies
This study focuses on creating a biobank that collects and stores human samples from both kidney transplant donors and recipients. It includes various types of biological specimens such as biopsy tissue, peripheral blood, and urine samples. The collected clinical data and bio-specimens will be used for future translational research projects aimed at improving kidney transplantation outcomes.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals who are either donors or recipients of renal transplants.
Not a fit: Patients who are not involved in kidney transplantation, such as those with other types of organ failure, may not benefit from this study.
Why it matters
Potential benefit: If successful, this biobank could enhance our understanding of kidney transplantation and lead to improved treatments and outcomes for patients with kidney failure.
How similar studies have performed: Other studies involving biobanks for organ transplantation have shown promise in advancing research and improving patient care.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * renal transplant recipients/donors Exclusion Criteria: * none
Where this trial is running
Leuven, BE
- Department of Nephrology and Renal Transplantation - University Hospitals Leuven — Leuven, BE, Belgium (RECRUITING)
Study contacts
- Principal investigator: Maarten Naesens, MD, PhD — Universitaire Ziekenhuizen KU Leuven
- Study coordinator: Maarten Naesens, MD, PhD
- Email: maarten.naesens@uzleuven.be
- Phone: 32 16344580
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Kidney Failure