Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Shanghai, Shanghai Municipality, 200092, China
NCT Number: NCT05042245
This is a multicenter, randomized, double-blind, double-dummy, and positive control clinic trial which explores the efficacy and safety of ornithine aspartate granules in the treatment of non-alcoholic fatty liver disease against silymarin capsules. The hypothesis is that the ornithine aspartate granules have similar or better efficacy than the silymarin capsules.
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Notify Me18 year–65 year
All sexes
Interventional
Phase 4
Shanghai, Shanghai Municipality, 200092, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ornithine aspartate granules in the experimental arm.
Silymarin capsules in the active comparator arm.
Silymarin capsule simulant in the experimental arm.
Ornithine aspartate granule simulant in the active comparator arm.
Time frame: Assessed at 24 weeks
Time frame: Assessed at 4 weeks, 12 weeks, and 24 weeks
Time frame: Assessed at 4 weeks, 12 weeks, and 24 weeks
Time frame: Assessed at 4 weeks, 12 weeks, and 24 weeks
An exploratory indicator
Time frame: Assessed at 4 weeks, 12 weeks, and 24 weeks
An exploratory indicator of body composition analysis
Time frame: Assessed at 4 weeks, 12 weeks, and 24 weeks
An exploratory indicator of body composition analysis
Time frame: Assessed at 4 weeks, 12 weeks, and 24 weeks
An exploratory indicator of body composition analysis
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Other
The Efficacy and Safety of Ornithine Aspartic Acid Granules in Non-Alcoholic Fatty Liver Disease Against Silymarin Capsules: a Randomized, Double-Blind, Multicenter Clinical Trial
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