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Gastrostomy-Biliary Diversion: Innovative Management for Bile Canalicular Transport Disorders

Primary Purpose

Progressive Familial Intrahepatic Cholestasis

Status
Unknown status
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Gastostomy-biliary tube
External biliary diversion, internal biliary diversion and nasobiliary tube
Sponsored by
National Liver Institute, Egypt
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Progressive Familial Intrahepatic Cholestasis focused on measuring bile canalicular transport disorders

Eligibility Criteria

1 Year - 18 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • PFIC cases that are previously responding to medical treatment with recent flare of the disease that doesn't respond to medical therapy
  • PFIC cases that are not responding to medical treatment and refusing non-transplant surgery and not indicated for liver transplant
  • BRIC cases with frequent attacks not responding to medical therapy and refusing or unable to tolerate nasobiliary stent

Exclusion Criteria:

  • Severe portal hypertensive gastropathy
  • Decompensated cirrhosis

Sites / Locations

  • Pediatric Hepatology, Gastroenterology and Nutrition Department, National Liver Institute, Menoufia UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Gastrostomy-biliary tube

Other biliary diversion modalities

Arm Description

The study group will be subjected to gastrostomy followed by ERCP with nasobiliary stent placement in the CBD with its distal end been exit from the previously performed gastrostomy instead of the nostril

The control group will include those cases with other modalities of therapy as external biliary diversion, internal biliary diversion, and nasobiliary tube

Outcomes

Primary Outcome Measures

Occurrence of bleeding
number of patients with bleeding
Occurrence of infection
number of patients with infection

Secondary Outcome Measures

Serum bilirubin level
number of patients with normal bilirubin
Improvement of pruritus
number of patients with no pruritus

Full Information

First Posted
August 25, 2019
Last Updated
August 20, 2020
Sponsor
National Liver Institute, Egypt
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1. Study Identification

Unique Protocol Identification Number
NCT04071197
Brief Title
Gastrostomy-Biliary Diversion: Innovative Management for Bile Canalicular Transport Disorders
Official Title
Gastrostomy-Biliary Diversion: Innovative Management for Children With Bile Canalicular Transport Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 10, 2020 (Actual)
Primary Completion Date
October 1, 2020 (Anticipated)
Study Completion Date
April 1, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Liver Institute, Egypt

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Progressive familial intrahepatic cholestasis (PFIC) is a group of disorders that can present early in life with cholestasis and intractable pruritus. Their treatment poses a great challenge, with medical treatment is not successful in many cases. Moreover, the available non-transplant surgeries carry many side effects and different degrees of efficacy. Partial external biliary diversion, internal biliary diversion, and ileal exclusion still lack widespread experience with many side effects. Nasobiliary stent placement has little tolerability, especially in younger age. Gastrobiliary tube is a novel modality for external biliary diversion in such patients.
Detailed Description
Progressive familial intrahepatic cholestasis (PFIC) is a group of disorders that can present early in life with cholestasis and intractable pruritus. They result primarily from defective transporters of different bile constituents on the canalicular membrane. The mildest form of these defective transporters can present by what is called benign recurrent intrahepatic cholestasis (BRIC). More recently both disease categories that represent the severest (PFIC) and mildest (BRIC) forms of these transporters are better nomenclated as bile canalicular transport disorders, as some cases can start early as BRIC and later in life progress the PFIC phenotype. Moreover, a continuous spectrum of severity is present between what were previously known as PFIC and BRIC. If the severest forms are not treated effectively they can have devastating outcomes reaching death. On the other hand, those known as BRIC can have severe attacks with unremitting pruritus that could be prolonged and sometimes persistent. Their treatment poses a great challenge, with medical treatment is not successful in many cases. Moreover, the available non-transplant surgeries carry many side effects and different degrees of efficacy. Partial external biliary diversion is not always successful and has disfiguring effects and the stoma can have many side effects. Internal biliary diversion and ileal exclusion still lack widespread experience and encouraging results due to sometimes lack of efficacy and others due to side effects. Nasobiliary stent placement was tried in previous cases with a promising outcome, but with little tolerability, especially in younger age. In spite liver transplant is the last resort for failing cases, the availability of successful non transplant therapy would be the preferable one if it is with adequate efficacy and little side effects. The innovative intervention proposed in this study is expected to have a good efficacy due to total biliary diversion rather than the partial ones obtained by other surgeries. Moreover, it avoids the disfiguring impact of the jeujenal stoma. More importantly, it can be removed at any time and be used at the times of severe flare of the disease.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Progressive Familial Intrahepatic Cholestasis
Keywords
bile canalicular transport disorders

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study group will be subjected to gastrostomy followed by ERCP with nasobiliary stent placement in the CBD with its distal end been exit from the previously performed gastrostomy instead of the nostril
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Gastrostomy-biliary tube
Arm Type
Experimental
Arm Description
The study group will be subjected to gastrostomy followed by ERCP with nasobiliary stent placement in the CBD with its distal end been exit from the previously performed gastrostomy instead of the nostril
Arm Title
Other biliary diversion modalities
Arm Type
Experimental
Arm Description
The control group will include those cases with other modalities of therapy as external biliary diversion, internal biliary diversion, and nasobiliary tube
Intervention Type
Device
Intervention Name(s)
Gastostomy-biliary tube
Intervention Description
gastrostomy followed by ERCP with nasobiliary stent placement in the CBD with its distal end been exit from the previously performed gastrostomy instead of the nostril
Intervention Type
Device
Intervention Name(s)
External biliary diversion, internal biliary diversion and nasobiliary tube
Intervention Description
All biliary diversion modalities other than gastrobiliary tube
Primary Outcome Measure Information:
Title
Occurrence of bleeding
Description
number of patients with bleeding
Time Frame
6 months
Title
Occurrence of infection
Description
number of patients with infection
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Serum bilirubin level
Description
number of patients with normal bilirubin
Time Frame
12 months
Title
Improvement of pruritus
Description
number of patients with no pruritus
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: PFIC cases that are previously responding to medical treatment with recent flare of the disease that doesn't respond to medical therapy PFIC cases that are not responding to medical treatment and refusing non-transplant surgery and not indicated for liver transplant BRIC cases with frequent attacks not responding to medical therapy and refusing or unable to tolerate nasobiliary stent Exclusion Criteria: Severe portal hypertensive gastropathy Decompensated cirrhosis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ahmad M Sira, M.D.
Phone
+2-048-222-2740
Email
asira@liver.menofia.edu.eg; ahmadsira@hotmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ahmad M Sira, M.D.
Organizational Affiliation
Pediatric Hepatology Dep; National Liver Institute, Menoufia University, Egypt
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatric Hepatology, Gastroenterology and Nutrition Department, National Liver Institute, Menoufia University
City
Shibīn Al Kawm
State/Province
Menofiya
ZIP/Postal Code
32511
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ahmad M Sira, M.D.
Phone
+2-048-222-2740
Email
asira@liver.menofia.edu.eg; ahmadsira@hotmail.com
First Name & Middle Initial & Last Name & Degree
Hanaa A El-Araby, MD
First Name & Middle Initial & Last Name & Degree
Hosam-Eldin M Basiouny, MD
First Name & Middle Initial & Last Name & Degree
Hadeer S Allam, M.B.;B.Ch.
First Name & Middle Initial & Last Name & Degree
Esam A Elsheimy, MD

12. IPD Sharing Statement

Citations:
PubMed Identifier
20955958
Citation
van der Woerd WL, van Mil SW, Stapelbroek JM, Klomp LW, van de Graaf SF, Houwen RH. Familial cholestasis: progressive familial intrahepatic cholestasis, benign recurrent intrahepatic cholestasis and intrahepatic cholestasis of pregnancy. Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):541-53. doi: 10.1016/j.bpg.2010.07.010.
Results Reference
background
PubMed Identifier
21769524
Citation
Kaur S, Sharma D, Wadhwa N, Gupta S, Chowdhary SK, Sibal A. Therapeutic interventions in progressive familial intrahepatic cholestasis: experience from a tertiary care centre in north India. Indian J Pediatr. 2012 Feb;79(2):270-3. doi: 10.1007/s12098-011-0516-8. Epub 2011 Jul 19.
Results Reference
background
PubMed Identifier
22033772
Citation
Mochizuki K, Obatake M, Takatsuki M, Nakatomi A, Hayashi T, Okudaira S, Eguchi S. Partial internal biliary diversion for patients with progressive familial intrahepatic cholestasis type 1. Pediatr Surg Int. 2012 Jan;28(1):51-4. doi: 10.1007/s00383-011-3018-x.
Results Reference
background
PubMed Identifier
16374853
Citation
Stapelbroek JM, van Erpecum KJ, Klomp LW, Venneman NG, Schwartz TP, van Berge Henegouwen GP, Devlin J, van Nieuwkerk CM, Knisely AS, Houwen RH. Nasobiliary drainage induces long-lasting remission in benign recurrent intrahepatic cholestasis. Hepatology. 2006 Jan;43(1):51-3. doi: 10.1002/hep.20998.
Results Reference
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Gastrostomy-Biliary Diversion: Innovative Management for Bile Canalicular Transport Disorders

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