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Clinical Study of DAAs Combined with UC-MSCs in the Treatment of Decompensated Hepatic Cirrhosis Patients

Key project of disease prevention and control of science and technology department of Guangzhou Province: Clinical Study of DAAs Combined with UC-MSCs in the Treatment of Decompensated Hepatic Cirrhosis Patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17013613
Enrollment
Unknown
Registered
2017-11-30
Start date
2017-09-01
Completion date
Unknown
Last updated
2017-12-11

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

Conditions

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Interventions

B:DAAs combined with UC-MSCs
A:DAAs

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. male or female aged from 18 to 65 years; 2. The patients met the diagnostic criteria for hepatitis C according to the 2015 guidelines for the prevention and treatment of hepatitis C and met the following conditions of decompensation: (1) Child-puph B (7 - 9) or C (10 - 15); (2) any of evidence of chronic liver insufficiency: Hepatic encephalopathy; Serum total bilirubin >51umol/L; PT>5s d.serum albumin <28g/L; moderate or severe ascites; (3) happened esophagealgastricavariceal bleeding, spontaneous peritonitis. 3. The detection of HCV RNA was positive.

Exclusion criteria

Exclusion criteria: 1. History of antiviral, antitumor or immunosuppressive drugs use in the previous 6 monthes; 2. Pregnant or lactating women or a birth plan during treatment; 3. Co-infection with other viruses (hepatitis A, B or E, or HIV); 4. Other causes of chronic liver diseases (e.g., autoimmune liver disease, alcoholic liver disease, drug induced liver injury, hereditary metabolic liver disease,etc.); 5. Co-existing hepatocellular carcinoma or AFP >100 ng/mL; 6. Other malignancies; 7. Serious diseases in other organ systems (e.g.,renal impairment: urine proteinserum(+), creatinine>116umol/L, etc.); 8. Intolerance to the medical treatments mentioned above; 9. The patients who will receive bioartificial liver support therapy or liver transplantation; 10. Disagreement to informed consent; 11. The researchers considered inappropriate to participate in the study because of other reasons.

Design outcomes

Primary

MeasureTime frame
MELD;

Countries

China

Contacts

Public ContactXiaohong Zhang

The Third Affiliated Hospital of Sun Yat-sen University

zhangxh5@mail.sysu.edu.cn+86 18922103273

Outcome results

None listed

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