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Efficacy and safety of Human Bone Marrow Derived Mesenchymal in Patients with pre-acute-on-chronic liver failure

Efficacy and safety of Human Bone Marrow Derived Mesenchymal in Patients with pre-acute-on-chronic liver failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116016
Enrollment
Unknown
Registered
2026-01-04
Start date
2026-01-04
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Pre-acute-on-chronic liver failure

Interventions

Bone marrow mesenchymal stem cell treatment group:CG-BM1 allogeneic human bone marrow mesenchymal stem cell injection
Standardized drug treatment group:CG-BM1 allogeneic human bone marrow mesenchymal stem cell injection

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18 to 60 years old; 2. Meet the pre-diagnosis criteria for liver failure as stipulated in the "Guidelines for the Diagnosis and Treatment of Liver Failure (2024 Edition)" : 1) Extreme fatigue, accompanied by obvious anorexia, vomiting, abdominal distension and other severe digestive tract symptoms; 2) Significant increase in ALT and/or AST, progressive deepening of jaundice (85.5µmol/L = 17.1µmol/L; There is a bleeding tendency, 40% < PTA <= 50%(PT INR < 1.5). 3. The subjects voluntarily participated in this study and have signed the informed consent form by themselves or their guardians.

Exclusion criteria

Exclusion criteria: 1.Pregnancy, preparation for pregnancy or lactation; 2.Individuals with neurological or psychiatric disorders who are unable to cooperate or unwilling to cooperate; 3.Severe chronic non-liver organ failure; 4.Untreated HIV infection; 5.Infection with hemodynamic instability; 6.Diagnosed hepatocellular carcinoma or other malignant tumors of organs during screening; 7.Previously participated in clinical trials on stem cells; 8.Participants who are currently participating in other clinical trials or have participated in other clinical trials within 3 months; 9.Not willing to sign informed consent form;

Design outcomes

Primary

MeasureTime frame
Survival rates at day 90;

Secondary

MeasureTime frame
Rates of ACLF at Day 28;

Countries

China

Contacts

Public ContactHe Yingli

The First Affiliated Hospital of Xi'an Jiaotong University

heyingli2000@xjtu.edu.cn+86 29 8532 4016

Outcome results

None listed

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