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Clinical Evaluation of the Efficacy of Dietary Sulforaphane on Male Fatty Liver Patients with Liver Dysfunctio

Not Applicable
Conditions
Abnormality of liver function
Registration Number
JPRN-UMIN000012855
Lead Sponsor
Tokai University School of Medicine
Brief Summary

Dietary supplementation with sulforaphane precursor glucoraphanin for 2 months significantly decreased serum levels of liver function markers, ALT and g-GTP, and an established oxidative stress marker, urinary level of 8-OHdG. The reduction of urinary 8-OHdG was significantly correlated with decreased levels of both ALT and g-GTP.

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

We will exclude outpatients 1) with serious liver diseases and suspected acute liver failure. 2) with viral hepatitis 3) with serious heart problem 4) with renal dysfunction (serum creatinine > 2.0 mg/dL) 5) with bile duct cancer 6) without capacity of self- management of drug therapy 7) with serious diseases in their life and then judged unsuitable for this study 8) with risk of allergy 9) with suspected infectious diseases 10) who participated in other clinical trials within 2 months. 11) who habitually consume higher amount of alcohol (> avg 60 g alcohol/day) 12) who are judged unsuitable for this study by principal investigator

Study & Design

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