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The effects of Umbilical cord blood stem cells in treatment of patients with decompensated HBV-associated live cirrhosis: a randomized controlled trial

The effects of Umbilical cord blood stem cells in treatment of patients with decompensated HBV-associated live cirrhosis: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004411
Enrollment
Unknown
Registered
2014-02-23
Start date
2014-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Liver cirrhosis

Interventions

Treatment group:Umbilical cord blood stem cells
Control group:0.9% Sodium chloride containing 1% Human Albumin

Sponsors

Taihe Hospital, Hubei University of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. A history of chronic HBV infection; 2. Ultrasonographic evidence of LC; 3. HBV DNA >100 IU/ ml; 4. CTP Score more than 7.

Exclusion criteria

Exclusion criteria: 1. The presence of HCC and any underlying neoplasm; 2. Liver failure (TBil>10 ULN, PTA<40%); 3. A history of variceal bleeding 2 months prior to the enrolment; 4. The presence of severe comorbidities; 5. Coinfection with HAV, HCV, HDV, HEV, HIV, etc; 6. Evidence of extrahepatic biliary diseases; 7. The presence of hepatic, portal, or splenic vein thromboses on Doppler ultrasonography; 8. Active substance abuse; 9. A history of nucleot(s)ides administration 6 months prior to the enrolment; 10. Unwillingness to sign the informed consent form.

Design outcomes

Primary

MeasureTime frame
Liver function;liver stiffnes;

Secondary

MeasureTime frame
HBV DNA;

Countries

China

Contacts

Public ContactZhongji Meng

Taihe Hospital, Hubei University of Medicine

zhongji.meng@163.com+86 071 98801821

Outcome results

None listed

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