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HEPANTIVIR CLINICAL TRIA

Not Applicable
Conditions
HEPATITIS
Registration Number
PACTR201507001055177
Lead Sponsor
BOLAR PHARMACEUTICALS LTD
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
50
Inclusion Criteria

Fifty consecutive and consenting patients being managed by gastroenterology unitwith clinical and biochemical features as well as serological evidence of chronic hepatitis B infection and who meet the study criteria- 18 years and above, HBsAg positive with elevated serum ALT, Serum HBV DNA > 2000iu/ml

Exclusion Criteria

No consent, presence of underlying liver malignancy, presence of co-morbidities eg end-organ failure

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
improvement in symptoms, laboratory measurement including transaminase and HBV load as well as any adverse event will be compared between the treatment arm and tenofovir using chi sqaure test.
Secondary Outcome Measures
NameTimeMethod
Absence of HBV DNA
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