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Clinical Trials/CTRI/2018/03/012644
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.

Registry
who.int
Start Date
TBD
End Date
May 16, 2018
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Apex Laboratories

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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