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A CLINICAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF Oâ??LIVER -T IN PATIENTS WITH HEPATITIS A VIRUS.

Not Applicable
Completed
Conditions
Health Condition 1: B15- Acute hepatitis A
Registration Number
CTRI/2015/01/005395
Lead Sponsor
SBL PVT LTD
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

•Male and female subjects18- 40 years of age

•Patients having acute virus A hepatitis in the serum.

•Willing to provide written informed consent along with audio video visual

•Subjects willing to comply with all the study procedure and requirements

Exclusion Criteria

•Who had HBsAg in the serum

•Patients who had history of ingesting hepatotoxic drugs prior to the onset of symptoms.

•Women with childbearing Potential and insufficient contraception.

•Female who is pregnant, planning a Pregnancy (during the course of the study) or

nursing a child.

•Any contraindication to blood sampling.

•History of HIV Positive serology.

Study & Design

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