Primary Prophylaxis for Variceal Bleed in Biliary Atresia (BA-BB)
Portal Hypertension, Biliary Atresia
About this trial
This is an interventional prevention trial for Portal Hypertension, Biliary Atresia focused on measuring Variceal bleed, primary prophylaxis, Biliary atresia
Eligibility Criteria
Inclusion Criteria: Infants and children with biliary atresia from 6 months to 5 years of age fulfilling either of the following conditions:
i. With unsuccessful Kasai portoenterostomy procedure with a bilirubin >2 mg/dL, or ii. Who did not underwent Kasai portoenterostomy, or iii. With successful Kasai portoenterostomy procedure with a bilirubin <2 mg/dL, but with features of portal hypertension i.e. clinical splenomegaly and/or thrombocytopenia (platelets < 1,00,000/mm3).
Exclusion Criteria:
i. History suggestive of hyper-reactive airway disease. ii. Congestive heart failure iii. Any degree of heart block (I,, II, III) iv. Infants and children already on beta-blockers in last 4 weeks. v. Portal vein atresia or thrombosis. vi. History of variceal bleed. vii. Infants and children on prophylactic or therapeutic endotherapy (band ligation or sclerotherapy).
viii. Potential liver transplant within 1 month.
Sites / Locations
- Institute of Liver and Biliary SciencesRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Propanolol
Placebo
Dose: 1 to 8 mg/kg/day in 1 to 2 divided doses adjusted to achieve target reduction in resting heart rate by 25% from baseline Frequency: once to Twice daily Route of Administration: Oral Duration: 18 months
Placebo in a similar manner