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Clinical trial on the deep learning-based molecular prediction and multiple-modality risk prediction models of liver failure and its critical complications

Clinical trial on the deep learning-based molecular prediction and multiple-modality risk prediction models of liver failure and its critical complications

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100048638
Enrollment
Unknown
Registered
2021-07-12
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-03-21

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

Conditions

Liver failure

Interventions

group1:Prospective cohort of liver failure
group2:Prospective cohort of hepatitis B and liver cirrohsis
group 3:Prospective cohort of pre-liver failure

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Age 18-65 years old, gender is not limited; 2. Meet the diagnostic criteria of the 2018 China Guidelines for the Diagnosis and Treatment of Liver Failure; 3. Laboratory tests: jaundice: serum total bilirubin >= 171 umol/L and coagulation disorders [international normalized ratio (INR) >= 1.5 or prothrombin activity (PTA) < 40%]; 4. Ascites and/or hepatic encephalopathy: confirmed by physical examination; 5. Understand and voluntarily sign the informed consent form approved by the ethics committee; 6. Be able to comply with the research procedures and visit schedule prescribed by the protocol.

Exclusion criteria

Exclusion criteria: 1. Serious diseases of other systems; 2. Patients co-infected with other hepatitis viruses and other non-hepatotropic viruses; 3. Liver cancer patients; 4. Alcohol: history of drinking within 4 weeks; 5. History of taking hepatotoxic drugs and Chinese herbal medicines within 4 weeks; 6. Onset of autoimmune hepatitis or Wilson disease; 7. 3-month medical and surgical history; 8. Unknown liver toxicity factors; 9. There are any other factors that the investigator considers unsuitable for inclusion in this study or completion of the study.

Design outcomes

Primary

MeasureTime frame
3 month mortality;

Countries

China

Contacts

Public ContactFan Yuchen

Qilu Hospital of Shandong University

fanyuchen@sdu.edu.cn+86 531 82169593

Outcome results

None listed

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