MR-proADM as a Early Biomarker for DGF and AR in Kidney and Liver Transplantation

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorUniversity of Rome Tor Vergata

About this trial

To define the sensibility and the specificity of increased levels of MR-proADM for early, non-invasive, diagnosis of AR and DGF after kidney and liver transplantation creating a predictive model for related complications after kidney and liver transplantation based on the pre-operative and post-operative levels of MR-proADM and by a machine learning process.

Eligibility criteria

Qualifiers

Kidney transplant recipient at our Institution

Liver transplant recipient at our Institution

Disqualifiers

Re-transplantation

Dual kidney transplantation

Combined transplant (kidney-liver, kidney-pancreas)

Autoimmune disease as indication to transplant

Trial design

Treatments tested in this trial

  • MR-proADM dosage

Treatment groups

300 Participants
are divided into 2 treatment groups

Sponsors and collaborators