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Improvement of nonalcoholic fatty liver disease by pig placenta extract (PPE) supplementation-Pilot study

Phase 1
Recruiting
Conditions
onalcoholic fatty liver disease
Registration Number
JPRN-jRCTs041210149
Lead Sponsor
Mutsumi Tsuchishima
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

1) Nonalcoholic fatty liver disease
2) Consent is obtained in writing
3) BMI: 25kg/m2 or more
4) Drinking amount: less than 20g/day (600g/month)

Exclusion Criteria

1) Those who are allergic to pig placenta preparations
2) Pregnant or nursing mothers
3) Patients with severe liver disease (decompensated cirrhosis: Child-Pugh grade C, Hepatocellular carcinoma)
4) Those who cannot ingest pigs religiously
5) Patients judged by the principal investigator or sub-investigator to be inappropriate as research subjects

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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