Freqency of Carnitine Deficiency in Patients with Chronic Liver Disease, and Efficacy of Oral L-Carnitine Treatment for Patiens with Liver Cirrhosis
Not Applicable
- Conditions
- Simple fatty liver, non-alcohoic steatohepatitis, alcoholic liver disease, and liver cirrhosis
- Registration Number
- JPRN-UMIN000013787
- Lead Sponsor
- Kansai Study Group of Liver Steatosis(KASALS)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 80
Inclusion Criteria
Not provided
Exclusion Criteria
1) Pregnant and lactating females 2) Hisotry of drug allergy 3) Inappropriate for entry onto this study in the judgment of the investigator 4) Administration of other test drugs within 1 month
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method