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 type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | University Hospital, Martin Academic / other |
| Locations | 1 site (Martin) |
| Status | Recruiting |
| Started | November 26, 2024 |
| Main results expected | November 26, 2026 |
| Study ends | November 26, 2027 |
| Registry record updated | December 10, 2025 |
| Trial ID | NCT07275541 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
- Study coordinator: Timea Blichova, MD
- Email: tc@unm.sk
- Phone: +421434203184
Similar studies
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.