CTRI/2018/03/012644
Completed
Phase 2
A Randomized Clinical End Point Study To Evaluate The Safety And Efficacy Of CLEARLIV Tablets In Patients With Alcoholic Liver Disease. - ALD
Apex Laboratories0 sites24 target enrollmentTBD
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Alcoholic Liver Disease patients
- Sponsor
- Apex Laboratories
- Enrollment
- 24
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Chronic alcohol intake patients
- •2\.Serum AST \&ALT is typically elevated to a level of 2â??6 times the upper limits of the normal.
- •3\.Negative pregnancy test for women in reproductive age (up to two weeks prior to the study)
- •4\.Negative for hepatitis B and C
Exclusion Criteria
- •1\.Patients who have liver disease with the cause different from that of alcohol induced liver disease.
- •2\.Drug dependence
- •3\.A known hypersensitivity or allergy to any component of the drugs evaluated in the study.
Outcomes
Primary Outcomes
Not specified
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