the Correlation Between Non-invasive Indicators in Patients With Biliary Atresia

Sponsor
National Taiwan University Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT02848573
Collaborator
(none)
41

Study Details

Study Description

Brief Summary

we propose this study and try to find out possible clinical applicable non-invasive imaging indices or its combination with the laboratory indices to predict the status of hepatic fibrosis in BA patients.

Study Design

Study Type:
Observational
Actual Enrollment :
41 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
the Correlation Between Hepatic Fibrotic Scores and ADC and Other Non-invasive Indicators in Patients With Biliary Atresia
Study Start Date :
Apr 1, 2008
Actual Primary Completion Date :
Jun 1, 2016

Outcome Measures

Primary Outcome Measures

  1. pathologic METAVIR fibrosis score [1 month]

Eligibility Criteria

Criteria

Ages Eligible for Study:
10 Days to 30 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • pathological proved diagnosis of biliary atresia, and without other distinct abnormality or malformations. All had undergone Kasai portoenterostomy. All of them received abdominal MRI study.
Exclusion Criteria:
  • absence of laboratory data required.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • National Taiwan University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
National Taiwan University Hospital, Assistant Professor, National Taiwan University Hospital
ClinicalTrials.gov Identifier:
NCT02848573
Other Study ID Numbers:
  • 201403098RINC
First Posted:
Jul 28, 2016
Last Update Posted:
Jul 28, 2016
Last Verified:
Jul 1, 2016
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 28, 2016