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Premature Infants with Biliary Atresia, a Nationwide Cohort Analysis

Premature Infants with Biliary Atresia, a Nationwide Cohort Analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON21672
Enrollment
30
Registered
2016-10-18
Start date
2016-10-18
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Describe the incidence and course of disease in premature infants with biliary atresia

Interventions

None

Sponsors

No funds received
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All premature infants treated for BA in the UMCG between 1987 and 2016

Exclusion criteria

Exclusion criteria: No treatment for BA, no premee.

Design outcomes

Primary

MeasureTime frame
Native liver survival, clearance of jaundice, mortality

Secondary

MeasureTime frame
Presence of congenital anomalies, age at onset of jaundice, age at onset of pale stool, age at presentation in first (community) hospital, referral interval (defined as days between presentation at first (community) hospital and KPE), age at KPE, corrected age at KPE,

Contacts

Public ContactDaan BE van Wessel

Parkweg 105

d.b.e.van.wessel@umcg.nl00316 40 61 16 61

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)