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The effect of Atorvastatin in combination to Tenofovir in the treatment of Hepatitis B

Phase 2
Conditions
iver Disease.
Toxic liver disease with hepatitis, not elsewhere classified
K71.6
Registration Number
IRCT20110621006852N2
Lead Sponsor
Ghoum University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
43
Inclusion Criteria

Patients with active hepatitis B that are candidates for anti-viral therapy
Viral load greater than 100,000 per ml
patients with elevated ALT

Exclusion Criteria

All patients with severe kidney failure.
Patients who use suppressor drugs for immune system.
Patients with acquired or congenital immune deficiencies.
Patients who have had a history of taking statins or any other antiviral medicines in the last six months.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Viral load. Timepoint: At the beginning of the trial and then once every three months interval. Method of measurement: realtime PCR.
Secondary Outcome Measures
NameTimeMethod
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