Monitoring molecular changes after kidney transplantation

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study focuses on the molecular monitoring of patients who have undergone kidney transplantation. It evaluates blood, plasma, urine, and tissue samples to assess the effectiveness of noninvasive diagnostic techniques in improving transplant outcomes. The study involves routine clinical and laboratory data collection at various time points post-transplantation, analyzing gene transcripts and conducting proteomic analyses. The goal is to identify biomarkers that could indicate the success of the transplant and potential complications.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Patients after kidney transplantation, male, female, informed consent

Exclusion Criteria:

* Deny of informed consent

Where it's running

• Odense University Hospital
  Odense, Dk, Denmark Recruiting

Study contacts

• Principal investigator: Martin Tepel, Dr — Odense University Hospital

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.