with the introduction of Direct-acting antiviral agents in the management of HCV, the scope of inclusion criteria had been widened to include patients with compensated cirrhosis and even in special situations patients with decompensated liver disease; a chance that was not offered by the limited and strict inclusion criteria needed for treatment by pegylated interferon-based regimen. this made the number of patients with progressive liver fibrosis of cirrhosis had been inv=creased even after achieving SVR. the debate about the impact of SVR on halting fibrosis progression had risen; some studies postulated that patients benefit from an SVR through reduction of mortality, morbidity, and improved quality of life ; however, some patients may maintain their level of fibrosis or even progress to cirrhosis despite achieving SVR and the risk for HCC remains even after virologic eradication.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
400
silymarin 140 three times daily
Ursodeoxycholic Acid 500
Beta Carotene - 6Mg Vitamin C - 200Mg Vitamin E - 50Mg
Colchicine 0.6
follow up by abdominal ultrasound and fibroscan every 6 month for 1 year
Improvement in liver stiffness measurement by Fibroscan
Liver stiffness assessment by Fibroscan every 6 months
Time frame: 1 year
Improved portal hypertension parameters
Assessment of portal vein diameter, splenic vein diameter, portal vein congestive index by ultrasound and Doppler every 6 months
Time frame: 1 year
Improved splenic stiffness measurement
assessment by ultrasound and fibroscan
Time frame: 1 year
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