Actively Recruiting

Age: 18Years +
All Genders
NCT07055984

Predicting Outcomes in Posttransplant Diabetes Mellitus Via microRNA

Led by University Hospital, Martin · Updated on 2025-07-09

130

Participants Needed

2

Research Sites

208 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The study aims to improve the prediction and early detection of post-transplant diabetes mellitus (PTDM) in kidney transplant recipients. The investigators are investigating whether specific microRNA profiles measured 3 months after transplantation can reliably predict the development of PTDM within the following one to two years. Additionally, the investigators are evaluating how traditional risk factors-such as age, immunosuppressive therapy, obesity, and infections like CMV-interact with these microRNA markers. The ultimate goal of this research is to identify early indicators of blood sugar issues, enabling timely interventions to improve health outcomes and personalize patient care after kidney transplantation.

CONDITIONS

Official Title

Predicting Outcomes in Posttransplant Diabetes Mellitus Via microRNA

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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.
Not Eligible

You will not qualify if you...

  • 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.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

Transplant-nephorlogy department

Martin, Slovakia, 03601

Actively Recruiting

2

University hospital Martin

Martin, Slovakia, 03601

Actively Recruiting

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Research Team

I

Ivana Dedinska, prof, MD, PhD.

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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