Last updated: April 11, 2023
Sponsor: Sheba Medical Center
Overall Status: Active - Enrolling
Phase
N/A
Condition
Primary Biliary Cholangitis
Liver Disease
Treatment
N/AClinical Study ID
NCT05676177
9785-22-SMC
Ages > 18 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria: Adult patients (age ≥18 years)
- At risk for hepatic steatosis (defined as at least one of the followings: age >50years, over weight (BMI>25), impaired fasting glucose or impaired glucose tolerance,T2DM, gestational diabetes, hyperlipidemia, hypertension, elevated liver enzymes,family history of steatosis or cirrhosis, increased liver span per medicalexamination, increased ferritin levels and the patatin-like phospholipasedomain-containing 3 polymorphism), as decided by the treating endocrinologist in ourinstitute's Medical screening department. 12-14
- No history of malignancy involving the liver.
- No known risk factors for hepatic iron deposition (multiple prior blood transfusions,known hemochromatosis).
- Subjects able to understand study procedures and provide informed consent.
- Subjects able to hold their breath during CT and MRI scans.
Exclusion
Exclusion Criteria: Patients younger than 18 years.
- Patients with risk factors from hepatic iron deposition (multiple prior bloodtransfusions, known hemochromatosis).
- Patients with known malignancy that involves the liver.
- Patients unable to hold their breath for both CT and MRI.
- Patients with severe claustrophobia.
- Patients with implanted devices of shrapnel.
- Pregnant people
Study Design
Total Participants: 150
Study Start date:
January 29, 2023
Estimated Completion Date:
December 31, 2025
Study Description
Connect with a study center
Prof. Noam Tau
Ramat Gan,
IsraelSite Not Available
Not the study for you?
Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.