Evaluation of Gd-EOB-DTPA MRI for Detection and Characterization of Liver Nodules in Cirrhotic Patients Undergoing Liver Transplantation and Potential Impact on Transplant Eligibility
Hepatocellular Carcinoma
About this trial
This is an interventional diagnostic trial for Hepatocellular Carcinoma focused on measuring Cirrhosis, HCC, Primovist
Eligibility Criteria
Inclusion Criteria:
a. Patients with liver cirrhosis enlisted for liver transplantation with high probability of undergoing transplantation within the ensuing 12 months
b. Patients who are diagnosed or suspected with HCC and listed for liver transplant surgery with priority MELD (Model for End-Stage Liver Disease) points based on the cancer diagnosis, regardless of whether they have or have not received pre-transplant treatments (incl. RFA, TACE, and XRT)
c. Subjects must be able to undergo MRI
Exclusion Criteria:
a. GFR <30 mL/min/1.73 m2
b. Elevated bilirubin (>3mg/dl)
c. Pregnant and/or nursing women
d. Contraindications to MRI such as pacemaker or ferromagnetic implants
e. Hypersensitivity to Primovist or to any ingredient in the formulation or component of the container
f. Younger than 18 years of age
Sites / Locations
- University Health NetworkRecruiting
Arms of the Study
Arm 1
Other
Single Arm
In this project, there is only one study group which comprises of patients with Hepatocellular Carcinoma (HCC) who will undergo Liver MRI with Primovist before hepatic transplantation.