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The role of intestinal flora in the occurrence of intrahepatic cholestasis during pregnancy and its clinical research

The role of intestinal flora in the occurrence of intrahepatic cholestasis during pregnancy and its clinical research

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100044540
Enrollment
Unknown
Registered
2021-03-23
Start date
2021-05-01
Completion date
Unknown
Last updated
2022-02-01

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:Nil
healthy control group:Nil

Sponsors

The Second Affiliated Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1.Patients aged 25 to 35 years with a clear diagnosis of intrahepatic stasis during pregnancy. 2.Volunteer to participate in and abide by the clinical trial protocol, sign a written informed consent form for the subjects, and receive review and follow-up on time.

Exclusion criteria

Exclusion criteria: 1. History of gastrointestinal surgery or other concomitant diseases. 2. There is a history of taking antibiotics in the past two months. 3. Those who are critically ill or suffer from physical and mental illness and cannot cooperate with the experiment. 4. The investigator believes that there are other patients who are not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
Microbiota;

Countries

China

Contacts

Public ContactYang Shiming

Department of Gastroenterology, the Second Affiliated Hospital of Army Medical University

13228686589@163.com+86 13228686589

Outcome results

None listed

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