Crassostrea Gigas for Liver Health

Status Not yet recruiting

Clinical Trial Summary

This study aimed to observe whether a hydrolyzed oyster extract improves liver health in participants whose alanine transaminase (ALT) levels are1-3 fold above the normal. A total of 96 participants will be randomly allocated to active (oyster) or placebo group (1:1). Each group will receive 750 mg of oyster extract or placebo per day for 8 weeks. Primary outcome will be the change in ALT level and secondary outcomes will be; (1) ratios of participants with normal ALT, aspartate aminotransferase (AST), and gamma-glutamyl transferase (GGT); (2) the change in serum bilirubin; (3) the change in multi-dimensional fatigue inventory; (4) the changes in serum lipids; (5) the changes in antioxidant enzymes.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Supportive Care

Related Conditions & MeSH terms

Fatty Liver
Non-alcoholic Fatty Liver Disease
Nonalcoholic Fatty Liver

Clinical Trial Details

NCT number	NCT02992470
Study type	Interventional
Source	Korean Medicine Hospital of Pusan National University
Contact	Jun-Yong Choi, PhD, KMD
Email	orientdoct@gmail.com
Status	Not yet recruiting
Phase	N/A
Start date	December 2016

View Details

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