* The study will be a prospective open labelled double blinded randomized controlled study. * The study will be conducted on patients admitted to Department of Hepatology from 2012 to 2014 at Institute of Liver and Biliary Sciences, New Delhi * Patients diagnosed as having clinical or subclinical hepatopulmonary syndrome will be started on oral pentoxifylline therapy 400 mg thrice daily for 12 weeks. * Patients not responding to this therapy will be given divided into 2 arms with one arm receiving additional Tab Rifaximin 400 mg thrice daily or placebo for 12 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
80
Tab Rifaximin 400 mg thrice daily + Pentoxifylline 400 mg thrice daily for 12 weeks
Tab Pentoxifylline 400 mg thrice daily + Placebo thrice daily for 12 weeks
Institute of Liver and Biliary Sciences
New Delhi, National Capital Territory of Delhi, India
RECRUITINGComplete response after 3 months of treatment
Time frame: 3 months
Development of serious adverse effects leading to withdrawal of the drug
Time frame: 3 months
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