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Recruiting NCT06830473

KTRSensor Scotland Study: An Observational Study Into Predictors and Diagnosis of Kidney Transplant Rejection

Observational Kidney Transplant Kidney Disease, Chronic

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: Kidney Transplant, Kidney Disease, Chronic. Basic parameters: 18 years — 99 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 Kingdom
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

KTRSensor Scotland Study: Investigating the Role of Biomarkers in Kidney Transplant Outcomes

Overview

An observational study capturing real world transplant patients in the post-operative setting aiming to further determine the utility of biomarkers to improve outcomes.

Detailed description

A prospective longitudinal observational study capturing patients receiving kidney transplants in Scotland. The primary objective is to assess whether there are clinical biomarkers present in the urine that determine the outcome of kidney transplants and predict early graft rejection.

Primary outcome measures

  • Number of participants that experience acute transplant rejection [Time frame: 12 months]

Eligibility criteria

Any patient within a Scottish Transplant centre who has undergone renal transplant (+/- pancreas/islet) and is due to attend routine follow-up appointments at the index centre.

Exclusion criteria

  • no previous kidney transplant
  • patient attending follow-up at a peripheral site
  • unable to provide urine samples across the study duration

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
Cohort

Study locations

United Kingdom · 2 centers
  • Royal Infirmary of Edinburgh — Edinburgh
  • Queen Elizabeth University Hospital — Glasgow

Identifiers

NCT: NCT06830473 · AC24216

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗