KCT0003058
Active, not recruiting
未知
A retrospective, observational study to evaluate the effectiveness of Carnitine complex (GODEX®) in patients with nonalcoholic fatty liver disease.
Celltrion Pharm0 sites30 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Celltrion Pharm
- Enrollment
- 30
- Status
- Active, not recruiting
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. 19 \~70 years old (Adult over 19 under the age of 70\)
- •2\. Subjects who were diagnosed with NAFLD
- •3\. If treated group, subjects who were treated with carnitine complex (824mg PO, TID) for at least 24 weeks form index date
- •4\. If control group, subjects who were not taking hepatotonic medications at least 24 weeks from index dates
Exclusion Criteria
- •1\. Chronic alcoholic disease
- •2\. Acute hepatitis A, Viral liver disease, drug induced liver disease, biliary obstruction (Chronic hepatitis B patients without taking antiviral agent are eligible)
- •3\. Subjects who administered oral hypoglycemic agent including insulin.
- •4\. Subjects who administered hyperlipidemia medication, antiobestic medication
- •5\. Subjects who administered hepatotonics except for carnitine complex (Godex cap.)
- •6\. Subjects with progressive diseases such as malignant tumor
- •7\. Subjects accompanying active hemorrhage
- •8\. Other subjects who are not eligible for this study
Outcomes
Primary Outcomes
Not specified
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