Indiana University
Indianapolis, Indiana, 46202, United States
NCT Number: NCT02654236
The main purpose of this study is to see whether heavy drinking will interfere with a specific pathway, called FXR signaling in the liver. The abnormality of this pathway may lead to liver injury in some patients who drink heavily.
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Notify Me21 year–65 year
All sexes
Interventional
Not applicable
Indianapolis, Indiana, 46202, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
1 tablet of placebo, taken orally daily with water, approximately 30 minutes prior to breakfast for 4 weeks.
10 mg Obeticholic Acid (OCA) Study medication will be administered orally, once daily, approximately 30 minutes prior to breakfast for 4 weeks.
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
This is the measurement to quantify two non-metabolized sugar molecules-lactulose and mannitol-to determine the gut permeability
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Time frame: Baseline to 28 days
Suthat Liangpunsakul
Other
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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