RecruitingNot ApplicableNCT04320199
Effect of Fermented Protaetia Brevitarsis Seulensis Powder on Alcohol-induced Liver Disease
Effect of Fermented Protaetia Brevitarsis Seulensis Powder on Alcohol-induced Liver Disease: a Randomized Controlled Trial
Sponsor
Pusan National University Yangsan Hospital
Enrollment
30 participants
Start Date
Jan 1, 2020
Study Type
INTERVENTIONAL
Conditions
Summary
The investigators conduct a randomized, double-blind, placebo-controlled study to investigate the effects of Fermented Protaetia brevitarsis seulensis powder on Alcohol-induced Liver Disease in adults for 8 weeks.
Eligibility
Min Age: 19 Years
Inclusion Criteria1
- Gamma-glutamyl transferase ranging from upper limit of reference to four times of upper limit
Exclusion Criteria8
- Abnormal liver or renal function (i.e., serum aminotransferase activity > 3 times of upper limit of reference range and serum creatinine concentrations > 1.2 mg/dL)
- Diabetes (diagnosed clinically or fasting glucose level > 126 mg/dL)
- History of viral hepatitis or cancer
- Uncontrolled hypertension
- History of serious cardiac disease such as angina or myocardial infarction
- History of gastrectomy
- History of medication for psychiatric disease
- Administration of oriental medicine including herbs within the past 4 weeks
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Interventions
DIETARY_SUPPLEMENTFermented Protaetia brevitarsis seulensis powder group
This group takes Fermented Protaetia brevitarsis seulensis powder for 8 weeks
DIETARY_SUPPLEMENTPlacebo group
This group takes placebo for 8 weeks
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04320199
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