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临床试验/NCT01724398
NCT01724398Unknown1 期

Safety and Efficacy of Human Umbilical Cord Mesenchymal Stem Cells Transplantation Combined With Plasma Exchange for Patients With Acute-on-Chronic Liver Failure Caused by Hepatitis B Virus (HBV)

Third Affiliated Hospital, Sun Yat-Sen University1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2012年11月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
120
试验地点
1
主要终点
Survival rate and time

研究概览

简要总结

Liver failure (LF) is a dramatic clinical syndrome with massive necrosis of liver cells. Although liver transplantation provides an option to cure patients suffering with LF, lack of donors, postoperative complications, especially rejection, and high cost limit its application. Previous study showed that bone marrow derived mesenchymal stem cells (BM-MSCs) the novel and promising therapeutic strategy, BM-MSCs can replace hepatocytes in injured liver, and effectively rescue experimental liver failure and contribute to liver regeneration. Plasma exchange (PE) can improve internal environment by removing endotoxin, it helps the liver regeneration and functional recovery and make UC-MSC differentiation into hepatocyte like cells, and exert immunomodulatory function. In this study, safety and efficacy of human umbilical cord mesenchymal stem cells (UC-MSCs) transplantation combined with plasma exchange (PE) for patients with liver failure caused by hepatitis B Virus will be evaluated.

详细描述

To investigate safety and efficacy of human umbilical cord mesenchymal stem cells (UC-MSCs) transplantation combined with plasma exchange (PE) for patients with liver failure caused by hepatitis B virus.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
16 Years 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Written informed consent
  • Acute-on-Chronic liver failure caused by hepatitis B virus
  • Model for End-Stage Liver Disease (MELD) <30

排除标准

  • Liver failure caused by other reasons, such as autoimmune diseases, alcohol, drug and so on
  • History of severe hepatic encephalopathy or variceal bleeding during the last two months before enrollment
  • Severe problems in other vital organs(e.g. the heart, renal or lungs)
  • Severe bacteria infection
  • Tumor on ultrasonography, CT or MRI examination
  • Pregnant or lactating women

结局指标

主要结局

Survival rate and time

时间窗: 48 weeks

次要结局

  • Improve biochemical indexes [alanine aminotransferase (ALT), albumin (ALB), total bilirubin (TBIL), prothrombin time (PT), INR and so on](24 weeks after treatment)
  • The clinical symptom improvement [including appetite, debilitation, abdominal distension, edema of lower limbs, et al](24 weeks after treatment)
  • Liver function evaluation using Child-Pugh score and MELD score(24 weeks after treatment)
  • Immune function improvement [including Th1/Th2](24 weeks after treatment)
  • The occurrence of complications [including body temperature, tetter and allergy](Between 0 to 8 hours after UC-MSCs transfusion)
  • Incidence of hepatocellular carcinoma(48 weeks after treatment)

研究者

发起方
Third Affiliated Hospital, Sun Yat-Sen University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Zhiliang Gao

Professor

Third Affiliated Hospital, Sun Yat-Sen University

研究点 (1)

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