Ireland
--:--IST
Active, not recruiting Observational

Observational Cohort Study Renal Transplantation University Hospitals Leuven

NCT06505200 · tracked via the Priya Life Science Belgium tracker
Phase
Observational
Started
2004-03-01
Last updated
2026-05-06

Condition(s) studied

Kidney Transplant RejectionKidney TransplantationKidney Transplant Failure

Investigational drug(s) / intervention(s)

No intervention

No intervention: No intervention

Study summary

This observational cohort study aims to compile routinely collected clinical, histological and outcome data of kidney transplant recipients, to evaluate risk factors for post-transplant injury, phenotypes of injury, and impact on outcome of such injury, in order to provide clinicians more accurate, less biased and faster tools for diagnosis, clinical management and treatment decisions with regard to kidney transplant rejection.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: \* All adult kidney transplant recipients transplanted at the University Hospitals Leuven between 01/03/2004 and 01/06/2022, without restrictions with regard to age, sex, underlying kidney disease etc. Exclusion Criteria: \* Patients with combined transplantations (e.g. heart + kidney, liver + kidney, lung + kidney)

Primary outcome measure(s)

  • Kidney transplant failure — 2004 - 2022
    Graft failure, recipient death

Trial sites (1)

FacilityCityRegionStatus
University Hospitals Leuven Leuven Belgium
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06505200 on ClinicalTrials.gov ↗ ← All trials in Belgium