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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02848573
Other study ID # 201403098RINC
Secondary ID
Status Completed
Phase N/A
First received July 26, 2016
Last updated July 26, 2016
Start date April 2008

Study information

Verified date July 2016
Source National Taiwan University Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan : Food and Drug Administration
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 41
Est. completion date
Est. primary completion date June 2016
Accepts healthy volunteers No
Gender Both
Age group N/A to 30 Years
Eligibility 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.

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms

  • Biliary Atresia
  • to Find Out Non-invasive Indices to Predict the Status of Hepatic Fibrosis in BA Patients.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
National Taiwan University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary pathologic METAVIR fibrosis score 1 month No