Clinical trial Recruiting at 1 site Observational Ages 18 and up

Platelet aggregation for diagnosing acute kidney transplant rejection

Official title: Platelet Aggregation in the Diagnosis of Acute Graft Rejection

Run by University Hospital, Martin · NCT07275541 · Data updated 2026-11-12

This study will test whether changes in platelet activation measured from blood can help detect acute rejection in adult kidney transplant recipients.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment60 (estimated)
SponsorUniversity Hospital, Martin
Academic / other
Locations1 site (Martin)
StatusRecruiting
StartedNovember 26, 2024
Main results expectedNovember 26, 2026
Study endsNovember 26, 2027
Registry record updatedDecember 10, 2025
Trial IDNCT07275541 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adult (≥18 years) primary kidney transplant recipients from living or deceased donors who can give informed consent and are not taking antiplatelet therapy are ideal candidates.

Probably not a fit

Patients on antiplatelet medications, those undergoing secondary or tertiary transplants, pediatric patients, or those unable to consent are unlikely to benefit from this protocol.

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

What this trial studies

This pilot observational study longitudinally measures platelet aggregation and activation markers in adult kidney transplant recipients before transplant and at protocol biopsies 3 and 12 months after transplant, and in patients undergoing indication biopsies for suspected graft dysfunction. Platelet function is measured by optical aggregometry, flow-cytometric P-selectin (CD62-P) expression, and soluble P-selectin levels. These platelet parameters are correlated with biopsy histology, donor-specific antibodies, metabolic data, and clinical outcomes. The goal is to determine whether platelet activation profiles can identify cellular or antibody-mediated rejection and support development of a non-invasive diagnostic tool.

Why it matters

Potential benefit: If successful, this approach could provide a non-invasive blood-based marker to detect acute kidney allograft rejection earlier and potentially reduce the need for some biopsies.

How similar studies have gone: Prior observational work has linked elevated platelet activation markers to rejection, but using platelet aggregation profiles as a diagnostic tool remains preliminary and is being tested in pilot studies.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* adult patients (≥18 years)
* primary kidney transplantation
* living / deceased donor kidney transplantation
* ability and consent to participate

Exclusion Criteria:

* non-adult patients
* secondary / tertiary kidney transplantation
* antiplatelet therapy
* patients unable to provide informed consent

Where it's running

  • Transplant-Nephrology Department, 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.