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临床试验/NCT02916641
NCT02916641Unknown3 期

Fuzhenghuayu for Patients With PBC Who Had An Inadequate Response to Ursodeoxycholic Acid

Xijing Hospital of Digestive Diseases1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2016年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
发起方
入组人数
200
试验地点
1
主要终点
Rate of patients with complete biochemical response

研究概览

简要总结

Ursodeoxycholic acid (UDCA) has been the only treatment for PBC approved by US and European drug administrations. Long-term use of UDCA(13-15 mg/kg/day) in patients with PBC improves serum liver biochemistries and survival free of liver transplantation However, about 40% of patients do not respond to UDCA optimally as assessed by known criteria for biochemical response. Those patients represent the group in need for additional therapies, having increased risk of disease progression and decreased survival free of liver transplantation. And UDCA has less effect on PBC patients whose pathology stage 3-4. Liver fibrosis might jeopardize the UDCA effect. Fuzhenghuayu is a Chinese traditional medicine for liver fibrosis and cirrhosis. Both lab research and some clinical studies suggest that Fuzhenghuayu could significantly reverse liver fibrosis and cirrhosis due to different kind of etiology. Here we start a random, open and parallel clinical research to explore the effect of Fuzhenghuayu combined with UDCA in the PBC treatment.

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
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Signed informed consent
  • Patient with PBC defined by 2 in 3 of the following criteria: a.Positive antimitochondrial antibody type M2; b.Abnormal serum alkaline phosphatases (ALP > 1,5N) and aminotransferase (AST or ALT > 1N) activities; c.Histological hepatic injuries consistent with PBC.
  • Had been treated with UDCA more than 6 months, and failed to achieve a complete biochemical response.

排除标准

  • Pregnancy or desire of pregnancy.
  • Breast-feeding.
  • Co-existing liver diseases such as acute or chronic viral hepatitis, alcoholic liver disease, choledocholithiasis, autoimmune hepatitis, biopsy-proven non-alcoholic fatty liver disease, Wilson's disease and hemochromatosis.
  • History or presence of hepatic decompensation (e.g., variceal bleeds, encephalopathy, or poorly controlled ascites).
  • History of urolithiasis, nephritis or renal failure (clearance of creatinine < 60 ml/mn).
  • Hepatotoxic drugs use before recruiting.
  • Fuzhenghuayu anaphylaxis.

研究组 & 干预措施

Fuzhenghuayu+UDCA

Experimental

Regular UDCA treatment combination with Fuzhenghuayu

干预措施: Fuzhenghuayu (Drug)

Fuzhenghuayu+UDCA

Experimental

Regular UDCA treatment combination with Fuzhenghuayu

干预措施: UDCA (Drug)

Monotherapy

Active Comparator

UDCA monotherapy

干预措施: UDCA (Drug)

结局指标

主要结局

Rate of patients with complete biochemical response

时间窗: Week 24

Normalization of alkaline phosphatase (ALP) or decrease of ALP by more than 40% compared to the baseline.

次要结局

  • Change in serum transaminase level(Weeks 0, 4, 8, 12, 24, and 48)
  • Change in liver biopsy examinations compared to the baseline.(Week 48)
  • Change in GLOBE scores after treatment.(Week 48)
  • Change in liver stiffness status measured by magnetic resonance elastography(Week 48)
  • Change in serum bilirubin level(Weeks 0, 4, 8, 12, 24, and 48)
  • Change in serum alkaline phosphatase (ALP) level(Weeks 0, 4, 8, 12, 24, and 48)

研究者

发起方
Xijing Hospital of Digestive Diseases
申办方类型
Other
责任方
Principal Investigator
主要研究者

Han Ying

Professor Consultant Physician

Xijing Hospital of Digestive Diseases

研究点 (1)

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