None listed
Conditions
Interventions
None listed
Sponsors
Catholic Kwandong University
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Adult men and women over 20 years of age 2) A person who has signed a written agreement with a description of the purpose and method of clinical research 3) Alcohol consumption is 30g or more per day for men and 20g or more per day for women. 4) Subjects without chronic hepatitis B, chronic hepatitis C, autoimmune hepatitis, primary biliary cirrhosis, and Wilson's disease
Exclusion criteria
Exclusion criteria: 1) women who are pregnant or lactating, whose pregnancies have been confirmed through pregnancy tests of serum or urine specimens, or who are planning a pregnancy during the test period, or who are pregnant but do not use approved methods of contraception 2) Those with bacterial inflammatory diseases other than alcoholic liver disease (eg, pneumonia, pyelonephritis, abscess, sepsis, etc.) 3) A person who has a history of hypersensitivity to a drug or its component 4) Those who have participated in other clinical studies within 60 days before enrollment in this clinical study 5) Others Judged by the tester as inappropriate for participation in clinical research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Before and after drinking, the fecal samples were collected from the intestinal microbiological environment | — |
Secondary
| Measure | Time frame |
|---|---|
| Imaging and hematologic changes after alcohol and alcohol treatment | — |
Countries
Korea, Republic of
Contacts
Public ContactSangheun Lee
Catholic Kwandong University International St.Mary's Hospital
Outcome results
None listed