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Primary Prophylaxis for Variceal Bleed in Biliary Atresia (BA-BB)

Primary Purpose

Portal Hypertension, Biliary Atresia

Status
Unknown status
Phase
Not Applicable
Locations
India
Study Type
Interventional
Intervention
Propanolol
Placebo
Sponsored by
Institute of Liver and Biliary Sciences, India
About
Eligibility
Locations
Arms
Outcomes
Full info

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

6 Months - 5 Years (Child)All SexesDoes not accept healthy volunteers

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

Arm Type

Experimental

Placebo Comparator

Arm Label

Propanolol

Placebo

Arm Description

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

Outcomes

Primary Outcome Measures

Bleeding free survival over 18 months follow-up

Secondary Outcome Measures

Progression, persistence or regression of esophageal varices
Progression, persistence or regression of gastric varices
Progression, persistence or regression of portal hypertensive gastropathy
Progression, persistence or regression of esophageal varices
Progression, persistence or regression of gastric varices
Progression, persistence or regression of portal hypertensive gastropathy
Progression, persistence or regression of esophageal varices
Progression, persistence or regression of gastric varices
Progression, persistence or regression of portal hypertensive gastropathy
Progression, persistence or regression of esophageal varices
Progression, persistence or regression of gastric varices
Progression, persistence or regression of portal hypertensive gastropathy
Overall survival
Overall survival
Overall survival

Full Information

First Posted
April 19, 2018
Last Updated
March 17, 2021
Sponsor
Institute of Liver and Biliary Sciences, India
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1. Study Identification

Unique Protocol Identification Number
NCT04494763
Brief Title
Primary Prophylaxis for Variceal Bleed in Biliary Atresia
Acronym
BA-BB
Official Title
Propanolol for Primary Prophylaxis for Variceal Bleed in Biliary Atresia - An Open Label Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2020
Overall Recruitment Status
Unknown status
Study Start Date
August 15, 2020 (Actual)
Primary Completion Date
June 13, 2022 (Anticipated)
Study Completion Date
June 15, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institute of Liver and Biliary Sciences, India

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Biliary atresia is the commonest etiology of neonatal cholestasis and is the most common indication for pediatric liver transplantation world-wide. Kasai-portoenterostomy (KPE) is the operative procedure of choice which helps in restoration of biliary flow and preventing rapid progression of fibrosis. Only 50-60% of infants have a successful surgery in terms of normalization of bilirubin (<2 mg/dL) after 3 months. Remaining 40-50% have rapid progression of PHT and eventual decompensation. Additionally, around 50-70% of infants with successful KPE have 1 or more episodes of cholangitis, and the severe ones if left untreated lead to progressive portal hypertension. Moreover in Indian setting a significant number of infants with biliary atresia reach late when the KPE is not feasible, and this group develops very rapid PHT and decompensation. Hence, overall around 70-80% of infants and children develop PHT within 5 years of age. Variceal bleed has been shown to be an important determinant of survival in infants with high bilirubin. Usage of beta-blockers in adult cirrhotics has been shown to reduce the progression of varices and incidence of variceal bleed. Although many pediatric hepatology centers worldwide use beta-blockers, there has been no controlled trial specifically to address this issue in children with biliary atresia. So, we planned this study to evaluate the efficacy of beta-blockers as primary prophylaxis for prevention of variceal bleed in biliary atresia children.
Detailed Description
(a) Aim and Objectives: Aim: To study the effect of beta-blockers for primary prophylaxis of variceal bleed in infants and children with biliary atresia. Primary objective: Bleeding free survival over 18 months FU Secondary objectives: (i) Progression, persistence or regression of esophageal and gastric varices, and portal hypertensive gastropathy over 3, 6, 12 and 18 months FU (ii) Overall survival at 18 months FU (b) Methodology: This will be an open label randomized controlled study where infants and children with biliary atresia from 6 months to 5 years fulfilling inclusion and exclusion criteria will be enrolled to receive propanolol or placebo for a duration of 18 months or till the occurrence of variceal bleed. i. Study design: Open label randomized controlled study with stratified randomization. ii. Intervention: Beta-blocker (Propanolol) versus placebo. iii. Study period: 1.5 years iv. Study population: Infants and children from 6 months to 5 years of age with Biliary atresia fulfilling the inclusion and exclusion criteria. (c) Expected outcome of the project: Beta-blockers reduce the incidence of variceal bleed in infants and children with biliary atresia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Portal Hypertension, Biliary Atresia
Keywords
Variceal bleed, primary prophylaxis, Biliary atresia

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Open label Randomized controlled trial - Block randomization
Masking
None (Open Label)
Allocation
Randomized
Enrollment
92 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Propanolol
Arm Type
Experimental
Arm Description
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
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo in a similar manner
Intervention Type
Drug
Intervention Name(s)
Propanolol
Intervention Description
Non-selective Beta-blocker
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Inactive drug
Primary Outcome Measure Information:
Title
Bleeding free survival over 18 months follow-up
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Progression, persistence or regression of esophageal varices
Time Frame
3 months
Title
Progression, persistence or regression of gastric varices
Time Frame
3 months
Title
Progression, persistence or regression of portal hypertensive gastropathy
Time Frame
3 months
Title
Progression, persistence or regression of esophageal varices
Time Frame
6 months
Title
Progression, persistence or regression of gastric varices
Time Frame
6 months
Title
Progression, persistence or regression of portal hypertensive gastropathy
Time Frame
6 months
Title
Progression, persistence or regression of esophageal varices
Time Frame
12 months
Title
Progression, persistence or regression of gastric varices
Time Frame
12 months
Title
Progression, persistence or regression of portal hypertensive gastropathy
Time Frame
12 months
Title
Progression, persistence or regression of esophageal varices
Time Frame
18 months
Title
Progression, persistence or regression of gastric varices
Time Frame
18 months
Title
Progression, persistence or regression of portal hypertensive gastropathy
Time Frame
18 months
Title
Overall survival
Time Frame
6 months
Title
Overall survival
Time Frame
12 months
Title
Overall survival
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
5 Years
Accepts Healthy Volunteers
No
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Rajeev Khanna, MD
Phone
+919654246963
Email
drrajeev_khanna@rediffmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rajeev Khanna, MD
Organizational Affiliation
Associate Professor, Pediatric Hepatology, Institute of Liver and Biliary Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Institute of Liver and Biliary Sciences
City
New Delhi
State/Province
Delhi
ZIP/Postal Code
110070
Country
India
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rajeev Khanna, MD
Phone
+919654246963
Email
drrajeev_khanna@rediffmail.com
First Name & Middle Initial & Last Name & Degree
Ankit Bhardwaj, MD
Phone
+9146300000
Email
bhardwaj.ankit3@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Endoscopic details of the patients on propanolol or placebo
Citations:
PubMed Identifier
27663417
Citation
Duche M, Ducot B, Ackermann O, Guerin F, Jacquemin E, Bernard O. Portal hypertension in children: High-risk varices, primary prophylaxis and consequences of bleeding. J Hepatol. 2017 Feb;66(2):320-327. doi: 10.1016/j.jhep.2016.09.006. Epub 2016 Sep 20.
Results Reference
background
PubMed Identifier
18223377
Citation
Fagundes ED, Ferreira AR, Roquete ML, Penna FJ, Goulart EM, Figueiredo Filho PP, Bittencourt PF, Carvalho SD, Albuquerque W. Clinical and laboratory predictors of esophageal varices in children and adolescents with portal hypertension syndrome. J Pediatr Gastroenterol Nutr. 2008 Feb;46(2):178-83. doi: 10.1097/MPG.0b013e318156ff07.
Results Reference
background
PubMed Identifier
17683492
Citation
Poddar U, Thapa BR, Rao KL, Singh K. Etiological spectrum of esophageal varices due to portal hypertension in Indian children: is it different from the West? J Gastroenterol Hepatol. 2008 Sep;23(9):1354-7. doi: 10.1111/j.1440-1746.2007.05102.x. Epub 2007 Aug 6.
Results Reference
background
PubMed Identifier
12198659
Citation
Zargar SA, Javid G, Khan BA, Yattoo GN, Shah AH, Gulzar GM, Singh J, Rehman BU, Din Z. Endoscopic ligation compared with sclerotherapy for bleeding esophageal varices in children with extrahepatic portal venous obstruction. Hepatology. 2002 Sep;36(3):666-72. doi: 10.1053/jhep.2002.35278.
Results Reference
background
PubMed Identifier
14731122
Citation
Zargar SA, Yattoo GN, Javid G, Khan BA, Shah AH, Shah NA, Gulzar GM, Singh J, Shafi HM. Fifteen-year follow up of endoscopic injection sclerotherapy in children with extrahepatic portal venous obstruction. J Gastroenterol Hepatol. 2004 Feb;19(2):139-45. doi: 10.1111/j.1440-1746.2004.03224.x.
Results Reference
background
PubMed Identifier
20637201
Citation
Duche M, Ducot B, Tournay E, Fabre M, Cohen J, Jacquemin E, Bernard O. Prognostic value of endoscopy in children with biliary atresia at risk for early development of varices and bleeding. Gastroenterology. 2010 Dec;139(6):1952-60. doi: 10.1053/j.gastro.2010.07.004. Epub 2010 Jul 14.
Results Reference
background
PubMed Identifier
23792202
Citation
Duche M, Ducot B, Ackermann O, Baujard C, Chevret L, Frank-Soltysiak M, Jacquemin E, Bernard O. Experience with endoscopic management of high-risk gastroesophageal varices, with and without bleeding, in children with biliary atresia. Gastroenterology. 2013 Oct;145(4):801-7. doi: 10.1053/j.gastro.2013.06.022. Epub 2013 Jun 19.
Results Reference
background
PubMed Identifier
10400097
Citation
Shashidhar H, Langhans N, Grand RJ. Propranolol in prevention of portal hypertensive hemorrhage in children: a pilot study. J Pediatr Gastroenterol Nutr. 1999 Jul;29(1):12-7. doi: 10.1097/00005176-199907000-00007.
Results Reference
background
PubMed Identifier
23266923
Citation
Drolet BA, Frommelt PC, Chamlin SL, Haggstrom A, Bauman NM, Chiu YE, Chun RH, Garzon MC, Holland KE, Liberman L, MacLellan-Tobert S, Mancini AJ, Metry D, Puttgen KB, Seefeldt M, Sidbury R, Ward KM, Blei F, Baselga E, Cassidy L, Darrow DH, Joachim S, Kwon EK, Martin K, Perkins J, Siegel DH, Boucek RJ, Frieden IJ. Initiation and use of propranolol for infantile hemangioma: report of a consensus conference. Pediatrics. 2013 Jan;131(1):128-40. doi: 10.1542/peds.2012-1691. Epub 2012 Dec 24.
Results Reference
background

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Primary Prophylaxis for Variceal Bleed in Biliary Atresia

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