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

Interested in this trial?

Get notified about updates and connect with the research team.

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)

Pusan National University Yangsan Hospital

Pusan, Ami-dong, South Korea

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT04320199


Related Trials