Liver Cirrhoses Clinical Trial
Official title:
"To Study the Impact of Balloon-occluded Retrograde Transvenous Obliteration (BRTO)/Plug Assisted Retrograde Transvenous Obliteration (PARTO) Mediated Portal Flow Modulation in Reduction of Ammonia and Improvement in Organ Volume and Functionality in Patients of Cirrhosis With LR Shunt - A Randomized Trial.ImPARTO Trial"
The informed consent will be obtained from the participants in the study. The study will be
conducted on indoor patients, Department of Hepatology ILBS, New Delhi. This will be a Pilot
study (sample size 25 cases in each arm) with 50% chances of each patient to randomized into
each arm(1:1 randomization) .
Study Population - Patients with hepatic encephalopathy with LR shunt admitted in wards/HDU
(High Dependency Unit)/LC ICU(Liver Coma ICU).
Study design-Randomized controlled Trial
Study period- 1 year.
Sample Size-Single Centre prospective RCT
- Sample size- Pilot study (sample size 25 cases in each arm)
- Follow up duration-6 months
n/a
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