Skip to content

Clinical database for prognostic study of liver failure: A bidirectional cohort study based on electronic medical records

Clinical database for prognostic study of liver failure: A bidirectional cohort study based on electronic medical records

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400084629
Enrollment
Unknown
Registered
2024-05-21
Start date
2024-06-01
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

liver failure

Interventions

A. Retrospective cohort:None (exemption from informed consent)
B. Prospective cohort:None (written informed consent required)

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: ACLF patients who meet the AARC ACLF criteria. Inclusion criteria: (1) Age 18-80 years old, male or female; (2) A history of chronic liver disease; (3) Total bilirubin =5 mg/dL (85 umol/L) and PT-INR =1.5, with or without cirrhosis and with or without prior decompensation of cirrhosis; (4) =24h of hospitalization (including emergency observation waiting for bed admission stage); (5) Informed consent: Informed consent is exempt from signing for database A (retrospective cohort database) of the clinical database on liver failure prognosis, and informed consent is required for database B (prospective cohort database).

Exclusion criteria

Exclusion criteria: (1) Pregnant women; (2) untreated HIV infection; (3) Malignant tumor history or suspected malignant tumor; (4) Plan to receive a non-liver organ transplant or have undergone any organ transplant.

Design outcomes

Primary

MeasureTime frame
Prognosis;

Secondary

MeasureTime frame
First artificial liver treatment time;Total number of artificial liver treatments;

Countries

China

Contacts

Public ContactYuanji Ma

West China Hospital of Sichuan University

maxe.doc@163.com+86 189 8060 6465

Outcome results

None listed

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