The relevant data will be prospectively collected included patient demographics, clinical, all laboratory variables including virological tests, genotyping by direct sequencing, abdominal ultrasound, and upper gastrointestinal (GI) endoscopy. Trans jugular liver biopsy (TJLB) and hepatic venous pressure gradient (HVPG) will be done in patients when it was not evident whether the underlying liver disease was chronic based on clinical, biochemical, radiological investigations, and upper GI endoscopy. Severity of the liver disease will be assessed by Child-Turcotte Pugh score (CTP) and model for end stage liver disease (MELD) score.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
69
Tenofovir (300 mg/day) plus telbivudine (600 mg/day).
In tenofovir arm subjects will receive tenofovir (300 mg) once daily.
Institute of Liver & Biliary Sciences (ILBS)
New Delhi, National Capital Territory of Delhi, India
Survival
Time frame: 1 and 3 months
Reduction in HBV DNA.
Time frame: 7 days, 15 days, 1 month and 3 month
Drug(s) related adverse effects/ side effects
Time frame: 1 and 3 months
Improvement in CTP and MELD scores
Time frame: 1 and 3 months
Alteration of renal functions
Time frame: 1 and 3 months
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