Traditional Chinese Medicine Combined With Entecavir to Treat Refractory Liver Fibrosis in Liver Cirrhosis Due to HBV

NCT02241616 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 350

Last updated 2018-10-15

No results posted yet for this study

Summary

Liver Cirrhosis is a common pathological consequence of chronic liver disease. Hepatitis B Virus (HBV) is one of most etiologies of Liver cirrhosis in China. The effective inhibition of HBV can partially regress or reverse liver fibrosis in patients with chronic Hepatitis and liver cirrhosis due to HBV, however some patients keep existence or development although HBV DNA is under-detectable after anti-virals. Theses refractory liver fibrosis is required the anti-fibrotic treatment focusing on the regulation of hepatic extracellular matrix, especially is necessary for in the patients with advance fibrosis stage ie. liver cirrhosis. Fuzheng Huayu has been found to enhance the degradation of collagens in fibrotic liver and have a good action against liver fibrosis in patients with chronic hepatitis B. However, there are no high quality clinical evidences which can demonstrate if the combination of anti-viral and anti-fibrotic therapy can improve the reversion of refractory liver fibrosis in liver cirrhosis due to HBV.

The primary objective of this study is to establish the safety and efficacy of the combination of Entecavir and Traditional Chinese Medicine in refractory liver fibrosis in liver cirrhosis due to HBV.

Conditions

  • Hepatitis B Virus Related Cirrhosis

Interventions

DRUG

Entecavir+Fuzheng Huayu+TCM Granule

The subjects will be taking 1 Entecavir tablet per day, 4 Fuzheng Huayu tablets three times a day and specific Traditional Chinese Medicine granule for 48 weeks.

Sponsors & Collaborators

  • Shanghai Zhongshan Hospital

    collaborator OTHER
  • Guangxi Ruikang Hospital

    collaborator OTHER
  • Hubei Hospital of Traditional Chinese Medicine

    collaborator OTHER
  • The First Affiliated Hospital of Hunan University of Traditional Chinese Medicine

    collaborator OTHER
  • Huai'an No. 4 People's Hospital

    collaborator UNKNOWN
  • Ruijin Hospital

    collaborator OTHER
  • Shenzhen Third People's Hospital

    collaborator OTHER
  • Beijing Ditan Hospital

    collaborator OTHER
  • Beijing YouAn Hospital

    collaborator OTHER
  • China-Japan Friendship Hospital

    collaborator OTHER
  • Tongji Hospital

    collaborator OTHER
  • Wenzhou Central Hospital

    collaborator OTHER
  • Jingmen No.1 People's Hospital

    collaborator OTHER
  • Affiliated Hospital of Shandong Univercity of TCM

    collaborator UNKNOWN
  • The Ninth Hospital of Nanchang

    collaborator OTHER
  • The People's Hospital of Ningxia

    collaborator OTHER
  • Fifth Hospital of Shijiazhuang City

    collaborator OTHER
  • The Fifth People's Hospital of Suzhou

    collaborator OTHER
  • The Fifth People's Hospital of Anyang

    collaborator UNKNOWN
  • ShuGuang Hospital

    lead OTHER

Principal Investigators

  • Chenghai Liu, PhD · ShuGuang Hospital

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2019-06-30
Completion
2019-06-30

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02241616 on ClinicalTrials.gov