Clinical trial Recruiting at 2 sites Observational Ages 18 and up

Predicting diabetes after kidney transplant using microRNA

Official title: Predicting Outcomes in Posttransplant Diabetes Mellitus Via microRNA

Run by University Hospital, Martin · NCT07055984 · Data updated 2026-11-12

We will test whether specific microRNA patterns measured three months after a kidney transplant can predict which adult transplant recipients will develop diabetes in the following one to two years.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment130 (estimated)
SponsorUniversity Hospital, Martin
Academic / other
Locations2 sites (Martin and 1 other locations)
StatusRecruiting
StartedApril 28, 2025
Main results expectedApril 28, 2028
Study endsApril 28, 2029
Registry record updatedJuly 9, 2025
Trial IDNCT07055984 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adult kidney transplant recipients without pre-existing type 1 or type 2 diabetes who can give informed consent and attend follow-up visits.

Probably not a fit

Patients with pre-existing diabetes, prior organ transplants, severe comorbidities that confound PTDM assessment (such as pancreatic disease), or inability to consent are unlikely to benefit from the study's predictive biomarkers.

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

What this trial studies

This observational study will collect blood samples from adult kidney transplant recipients without prior diabetes and measure microRNA profiles three months after transplantation. Participants will be followed for one to two years to record new-onset post-transplant diabetes mellitus (PTDM) and related clinical events. Researchers will combine microRNA data with traditional risk factors — including age, immunosuppressive regimen, obesity, and CMV infection — to develop predictive models. The aim is to find early molecular indicators that could prompt closer monitoring or preventive measures.

Why it matters

Potential benefit: If successful, the approach could allow earlier identification of patients at risk for post-transplant diabetes, enabling timely monitoring and individualized preventive steps to reduce complications.

How similar studies have gone: Some pilot studies have reported associations between microRNA signatures and diabetes risk after transplant, but larger validation studies remain limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult patients undergoing kidney transplantation.
* Absence of pre-existing type 1 or type 2 diabetes mellitus.
* Willingness to provide informed consent and comply with study procedures.

Exclusion Criteria:

* Pre-existing type 1 or type 2 diabetes mellitus.
* Previous organ transplantation.
* Severe comorbidities that could confound the assessment of PTDM (e.g., pancreatic disease).
* Inability to provide informed consent.

Where it's running

  • Transplant-nephorlogy department
    Martin, Slovakia
    Recruiting
  • University hospital Martin
    Martin, Slovakia
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.