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The association between total bile acid levels and adverse pregnant outcomes

The association between total bile acid levels and adverse fetal outcomes: a retrospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200062925
Enrollment
Unknown
Registered
2022-08-24
Start date
2022-08-25
Completion date
Unknown
Last updated
2023-04-12

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

Conditions

The hyperbileacidemia of Pregnancy

Interventions

TBA>=10umol/L:none

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Prenancy women were collected when TBA levels were >=10 mmol/L with or without signs of pruritus during pregnancy where found in the hospital records.

Exclusion criteria

Exclusion criteria: All pregnancies that were complicated by severe congenital malformations, which consisted of chromosomal abnormalities and/or multiple congenital anomalies, delieveried before 24 weeks, or deliveried in other hospitals were exclued in the study.

Design outcomes

Primary

MeasureTime frame
serum total bile acid;

Countries

China

Contacts

Public ContactYuzhu Yin
yinyuzhu@mail.sysu.edu.cn18922103157

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026