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Clinical Study on the Impact of Artificial Liver on Multiple Organ Failure in the Perioperative Period of Liver Transplantation for Liver Failure

Clinical Study on the Impact of Multiple Sessions of Artificial Liver on Multiple Organ Failure in the Perioperative Period of Liver Transplantation for Liver Failure

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600126241
Enrollment
Unknown
Registered
2026-06-05
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-06-08

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

Conditions

Perioperative Period of Liver Transplantation of liver failure

Interventions

Regular multiple artificial liver treatment group:Once every other day in the first week of enrollment, three times, once every 2-3 days in the second week, two times, and once a week from then to bef
On demand artificial liver treatment group:Once every week after enrollment until before liver transplantation

Sponsors

Fudan University Huashan Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients who are diagnosed with liver failure and are in the perioperative period of liver transplantation according to the diagnostic and therapeutic guidelines for liver failure (2024 Edition): severe liver injury caused by various reasons, resulting in serious impairment or decompensation of synthesis, detoxification, metabolism and biotransformation functions, blood coagulation disorders (INR >= 1.5), elevated total bilirubin (>= 10 mg/dl or >= 171 µ mol/l), with or without hepatic encephalopathy, hepatorenal syndrome, ascites, etc., meet the criteria for liver transplantation after liver transplantation evaluation (rapid progression of hepatic encephalopathy (grade II or above); Hepatorenal syndrome; Severe coagulation dysfunction (persistently elevated INR) or within 4 weeks after liver transplantation. 2. There was no limit on gender, and only adult cases were included, older than 18 years old and younger than or equal to 80 years old; 3. The patient and his family members understood and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with active bleeding and severe cardiac dysfunction or hemodynamic instability; 2. Participate in other clinical experiments at the same time; 3. Patients with severe allergy to blood products; 4. Female patients who are pregnant, lactating or planning pregnancy.

Design outcomes

Primary

MeasureTime frame
survival rate;

Secondary

MeasureTime frame
Incidence of multiple organ failure;Early allograft dysfunction;mechanical ventilation duration;Duration of vasoactive drug use;ICU stay;Postoperative complications;

Countries

China

Contacts

Public ContactZhu Xinfang

Fudan University Huashan Hospital

279676540@qq.com+86 21 5288 9556

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 11, 2026