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Cohort study of intrahepatic cholestasis of pregnancy

Cohort study of intrahepatic cholestasis of pregnancy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500098802
Enrollment
Unknown
Registered
2025-03-13
Start date
2025-03-16
Completion date
Unknown
Last updated
2025-03-17

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

Conditions

Intrahepatic Cholestasis of Pregnancy

Interventions

ICP group:None
Control group:None

Sponsors

Chengdu Women and Children's Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: Pregnant women with ICP; Agree to sign an informed consent form.

Exclusion criteria

Exclusion criteria: Patients with other comorbidities.

Design outcomes

Primary

MeasureTime frame
Bile acid;—

Secondary

MeasureTime frame
Maternal and infant complications;Preterm birth;—

Countries

China

Contacts

Public ContactXiao Yang

Chengdu Women and Children's Central Hospital

wcchgcptg@163.com+86 28 6186 6009

Outcome results

None listed

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