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Single-center Prospective Study of Non-invasive Methods for the Diagnosis of Postoperative Complications in Liver Transplant Recipients (ElastOLT)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Enrolling

Conditions

Rejection Acute Hepatic
Transplant; Failure, Liver
Liver Dysfunction

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

A lot of different early and late complications may occur after liver transplantation. They could be related to surgical procedure, to infectious diseases or immuno-mediated diseases (acute cellular rejection, ACR). Almost all of those complications are characterized by an elevation in liver enzymes (ALT, AST and GGT) and a decline of liver function tests (serum bilirubin and INR increase) possibly leading to early allograft disfunction (EAD). In this scenario there is a lack of biomarker that could predict the development of ACR and/or EAD.

The aim of this study is to explore the prognostic role of non-invasive instrumental and biological marker in the early post-transplant phase.

Enrollment

100 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients eligible for liver transplantation following National and International Guidelines

Exclusion criteria

  • No agreement or inability to give informed consent

    • Re-transplant patients
    • Liver transplant in fulminant hepatitis

Trial contacts and locations

1

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Central trial contact

Luca Miele, MD, PhD

Data sourced from clinicaltrials.gov

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