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Clinical Trials/KCT0002891
KCT0002891
Completed
未知

A human study for evaluating effectiveness and safety of barley sprout extracts consumption on alcoholic liver damage

Ewha Womans University0 sites76 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Ewha Womans University
Enrollment
76
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
June 4, 2021
Last Updated
4 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\) Subject who voluntarily agree to participate and signs informed consent form
  • 2\) 20 years\= Age (Ratio of men and women 1:1\)
  • 3\) Have been drinking alcohol more than a year as follows:
  • \- Men: more than 140g/week( about 2\.5 bottle as Soju, 2\.5glass/day)
  • \- Women: more than 70g/week( about a bottle as Soju, 1 glass/day)
  • 4\) Comply one of the following conditions
  • \- more than upper llimit of AST, AST:ALT ratio is 1
  • \- more than upper llimit of GGT
  • 5\) Confirmed a fatty liver

Exclusion Criteria

  • 1\) Usually drinking alcohol more than 350g/week( about 6 bottles/week, 6 glasses/day)
  • 2\) Exceed 3 times of normal upper limit more than one of the following categories: AST, ALT, GGT, total bilirubin
  • 3\) Have anamnesis in following diseases
  • ? Related to liver function
  • \- post\-transfusion hepatitis (hepatitis B surface antigen(HBsAg) or type C)
  • \- hepatic insufficiency, primary biliary cirrhosis
  • \- drug or surgery induced hepatitis
  • \- genetic liver disease
  • ? whole body infectious disease (include tuberculosis), serious cardiovascular or digestive system, thyroid disease, autoimmune disease, malignant tumor, multisystem failure, inflammatory enteropathy, a mental patient, confirmed as HIV\-positive.4\) Medical history of organ transplant or bone\-marrow transplantation
  • 5\) Consumption of sprout foods within 2 weeks before the first visit

Outcomes

Primary Outcomes

Not specified

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