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To evaluate the safety and Efficiency of Human Umbilical Cord Mesenchymal Stem Cell Transfusion in Patients with Decompensated Liver Cirrhosis: A Prospective, Multicenter Clinical Study

To evaluate the safety and Efficiency of Human Umbilical Cord Mesenchymal Stem Cell Transfusion in Patients with Decompensated Liver Cirrhosis: A Prospective, Multicenter Clinical Study

Status
Active, not recruiting
Phases
Phase 2
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800015304
Enrollment
Unknown
Registered
2018-03-21
Start date
2018-04-01
Completion date
Unknown
Last updated
2018-05-21

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

Conditions

Decompensated Liver Cirrhosis

Interventions

High dose group:Transfusion with high dose of MSC
Low dose group:Transfusion with low dose of MSC

Sponsors

Jinan Infectious Disease Hosptial
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Clinically diagnosed as decompensated liver cirrhosis; 2. Hepatitis B/C Liver Cirrhosis After Viral Treatment, HBV/HCV Viral Loads Below Detection Level over six mouths, and the liver function remained below Child-pugh A grade or MELD score >10; 3. Other causes of cirrhosis, liver function compensatory incomplete; 4. In the past year, despite active medical treatment taken, the condition has continued to increase, at least because of cirrhosis complications such as ascites, spontaneous peritonitis, gastrointestinal bleeding, and hepatic encephalopathy in hospital over one time; 5. Need to intermittently supplement albumin and apply diuretic therapy; 6. Albumin 30%; (Prothrombin time 5 points); 7. There was no history of gastrointestinal hemorrhage within the last month and population with no high-risk portal hypertension and gastrointestinal bleeding was evaluated recently; 8. Unconditional acceptance of orthotopic liver transplantation; 9. Aged from 18 to 65 years; 10. Voluntarily signed informed consent form.

Exclusion criteria

Exclusion criteria: 1. A malignant tumor with liver or other organs or a history of previous cancer; 2. Complications include gastrointestinal bleeding, spontaneous peritonitis, hepatic encephalopathy, hepatorenal syndrome, and Acute infection episodes; 3. Patients with severe heart, lung, kidney or blood system diseases and failure status; 4. Pregnant or lactating women; 5. Allergic constitution; 6. There is a history of alcohol abuse, drug abuse, and failure to effectively quit; 7. Patients did not participate in other clinical trials within 4 weeks; 8. Any condition, investigator believe that patients should not participate in this study.

Design outcomes

Primary

MeasureTime frame
Overall Survival;

Secondary

MeasureTime frame
Liver function;Liver ascites;MELD;Child-pugh;

Countries

China

Contacts

Public ContactJingbo Wang

Jinan Infectious Disease Hosptial

jingbocn@163.com+86 13335185669

Outcome results

None listed

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