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The evaluation of microbiome in liver abscess patients

Not Applicable
Conditions
Diseases of the digestive system
Registration Number
KCT0003857
Lead Sponsor
Catholic Kwandong University International St.Mary's Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
100
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) Patients requiring liver abscess drainage or fine-needle aspiration
4) Those who have participated in other clinical studies within 60 days before enrollment in this clinical study
5) A person who is judged to be inadequate in participating in clinical research

<control group>
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) A person whose alcohol intake is 30g or less for men or 20g or less for women.
4) Normal people without history of hypertension, diabetes and chronic hepatitis.
5) Without liver abscess and bacterial inflammatory disease (eg, pneumonia, pyelonephritis, abscess,

Exclusion Criteria

1) Patients who received antibiotics for the treatment of symptoms associated with liver abscess before participating in the clinical study
2) women who are pregnant or lactating, whose pregnancies have been confirmed by means of 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
3) Persons with bacterial inflammatory disease other than liver abscess (eg, pneumonia, pyelonephritis, abscess, sepsis, etc.)
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

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Differences in distribution of intestinal microorganisms
Secondary Outcome Measures
NameTimeMethod
iver enzyme levels and inflammatory response in blood
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