Surveys, Blood Testing, and Fibroscan in Screening for Liver Fibrosis and Liver Cirrhosis
Running, not enrolling · Not applicable
Conditions studied: Liver and Intrahepatic Bile Duct Carcinoma
In brief
This clinical trial studies the use of surveys, blood testing, and fibroscan in screening for liver fibrosis and liver cirrhosis in new or existing patients of the HOPE clinic seeking usual clinical care. Fibroscan is an imaging procedure of the liver which uses a probe like an ultrasound. Information gathered from this study may help researchers learn more about how to prevent or find liver cancer in patients who are currently receiving care at the HOPE clinic. Early detection of liver cancer may improve survival.
Key facts
- Study ID
- NCT04785534
- Run by
- M.D. Anderson Cancer Center
- People needed
- 1000
- Starts
- 2020-12-22
- Expected to finish
- 2026-08-31
- Last updated by the study team
- 2026-04-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Must be at least 18 years old
- Must be a new or existing patient of the HOPE clinic seeking usual clinical care
- Must be able to speak and read English or a language other than English for which there is a translator available on site at the HOPE clinic
You may not qualify if…
- Known pregnancy at time of recruitment. The HOPE clinic will ask the female patients if they are pregnant, will ask the participants for their last menstrual period (LMP), and/or they will use the urine pregnancy test (UPT) results in their electronic medical records
Where it is running
- M D Anderson Cancer Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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