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Recruiting NCT04272515

Molecular Characterization for Understanding Biliary Atresia

No phase Interventional Biliary Atresia

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: blood sampling, skin biopsy sampling, explanted liver of BA patients sampling.
Who it may be relevant to
Registry conditions: Biliary Atresia. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Although considered a rare disease, Biliary Atresia (BA) is the leading cause of neonatal cholestasis and liver transplantation in children. Little is known about the molecular mechanisms that drive BA. The purpose of this study is to collect the fluid samples, explanted liver tissue samples and dermal biopsy samples to enable investigators to perform the genetic and molecular analyses that might point to the gene(s) and cellular pathway involved in etiology of BA disease.

Detailed description

Biliary atresia (BA) is a disease characterized by intra- and extra-hepatic bile duct obstruction diagnosed in the neonatal period. If left untreated, this obstruction leads to biliary cirrhosis and early death. Although considered a rare disease (between 1/15,000 and 1/20000 births), it is the leading cause of neonatal cholestasis and liver transplantation in children. The reasons for this obstruction are still poorly known and might involve several factors (immune, infectious and possible toxin effect). The accumulating evidence point to genetic factors involved, yet they are not of the classic monogenic or Mendelian types. The purpose of this study is to collect the fluid samples, explanted liver tissue samples and dermal biopsy samples to enable investigators to perform the genetic and molecular analyses that might point to the gene(s) and cellular pathway involved in etiology of BA disease.

Interventions

  • Other blood sampling
    collection of blood sample for preparation of DNA
  • Other skin biopsy sampling
    preparation of primary cultures of dermal fibroblasts from skin biopsy sample
  • Other explanted liver of BA patients sampling
    cryoconservation of liver tissue for molecular analyses

Primary outcome measures

  • To identify the molecular mechanisms implicated in the etiology of BA [Time frame: 10 Years]

Eligibility criteria

Inclusion criteria

  • confirmed diagnosis of biliary atresia in patients
  • parents of BA patients

Exclusion criteria

  • no

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Basic science

Study locations

France · 2 centers
  • Hopital Necker enfants malades — Paris
  • PRC Inserm — Paris

Identifiers

NCT: NCT04272515 · C19-36

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗