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Clinical Trial Summary

This study measures the steatosis in patients With fatty livers as determined by CAP score from a fibroscan assessment. The study attempts to determine the effect of using the Medical Food Hepaxa in a Clinical setting Close to real-world use.


Clinical Trial Description

Subjects With fatty liver are given Hepaxa for 6 months. Fibroscan CAP measurements are taken at 3 monthly intervals. Subjects consent to Collection of data from approximately 6 months prior to use of Hepaxa. Patients unresponsive to life style recommendations given as standard practice will be enrolled. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03801577
Study type Interventional
Source BASF AS
Contact
Status Not yet recruiting
Phase N/A
Start date February 2019
Completion date December 2019

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