Changes in Glucose Tolerance in Patients With Cirrhosis Peri-Liver Transplant
Launched by UNIVERSITY OF CHICAGO · Apr 22, 2025
Trial Information
Current as of November 11, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is looking at how to predict the risk of developing diabetes in adults with cirrhosis who are preparing for a liver transplant. The researchers want to understand whether specific tests, such as blood tests, body measurements, and even devices that monitor glucose levels, can help identify which patients are more likely to face diabetes after their transplant.
To participate, you must be over 18 years old, have been diagnosed with cirrhosis, and be able to provide consent. If you join the study, you will wear a continuous glucose monitor and a wrist device that tracks your activity, and you will take a glucose tolerance test both before and after your transplant. This information can help doctors improve care for future liver transplant patients. Please note that some people, like those with certain medical devices or a history of diabetes diagnosed more than five years ago, may not be eligible to participate.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients presenting to liver transplant clinic with a diagnosis of cirrhosis.
- • Age \>18 yrs.
- • Ability to understand and sign written consent form, or have a legally-authorized representative or proxy who can be approached for consent
- Exclusion Criteria:
- • Patients without consent
- • Patients with implantable cardioverter defibrillator devices or automated implantable cardioverter defibrillator devices will be excluded from the bio-electrical impedance analysis portion of the measurements.
- • Patients with unremovable electrical medical devices or devices that cannot turn off will be excluded from the bio-electrical impedance analysis measurements
- • Pregnant patients
- • Incarcerated patients
- • Patients with a history of type 2 diabetes mellitus diagnosed \> 5 years ago will be excluded from the Oral Glucose Tolerance Test portion of the study
About University Of Chicago
The University of Chicago is a prestigious research institution renowned for its commitment to advancing medical science through innovative clinical trials. With a robust infrastructure that supports multidisciplinary collaboration, the University actively engages in cutting-edge research across various therapeutic areas. Its dedicated team of experienced investigators and state-of-the-art facilities enable the University of Chicago to conduct rigorous clinical studies aimed at improving patient outcomes and translating scientific discoveries into tangible healthcare solutions. The institution prioritizes ethical standards and patient safety, ensuring that all trials adhere to the highest regulatory guidelines and best practices in clinical research.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Chicago, Illinois, United States
Patients applied
Trial Officials
Mary E Rinella, MD
Principal Investigator
University of Chicago
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported