Status:
UNKNOWN
Treatment of Liver Cirrhosis Due to Hepatitis B Virus With Fuzheng Huayu and Entecavir
Lead Sponsor:
ShuGuang Hospital
Collaborating Sponsors:
Shanghai Zhongshan Hospital
Guangxi Ruikang Hospital
Conditions:
Liver Cirrhosis Due to Hepatitis B Virus
Eligibility:
All Genders
18-60 years
Phase:
PHASE4
Brief 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 partia...
Eligibility Criteria
Inclusion
- More than 6 months history of serum positive HBsAg
- Positive HBV-DNA
- Age 18-60
- Ishak fibrosis score of the biopsy within 6 months ≥5, no anti-virus or anti-fibrosis drug was taken within 6 months.
- Child-Pugh\<7 (Stage A)
- The patient or the patient's guardian agrees to participate the trial and sign the informed Consent Form.
Exclusion
- Primary Lamivudine, Adefovir dipivoxil and Entecavir resistance
- Decompensated liver cirrhosis
- HCC
- Liver histology conforming to other chronic liver diseases, such as moderate or severe non-alcoholic fatty liver disease(more than 1/3 steatosis in liver ), chronic hepatitis C, chronic hepatitis D, autoimmune hepatitis, primary biliary cholangitis, primary sclerosing cholangitis, inherited metabolic liver disease, drug or toxic induced liver injury, parasitic infections, alcoholic liver disease.
- Have psychiatric history or uncontrollable epilepsy patient.
- Uncontrollable diabetic patient
- History of hemoglobin disease (such as alpha- or beta-thalassemia, sickle cell disease, spherocytosis) or patients with toxic or autoimmune hemolytic anemia.
- Severe background disease like chronic respiratory failure, circulatory failure, kidney failure etc.
- In situ organ transplantation (such as liver, kidney, lung and heart) or bone marrow transplantation and stem cell transplantation.
- Immunocompromised patients: such as HIV infection or take immunosuppressor or glucocorticoid (such as cyclosporin, azathioprine, adrenocortical hormone) within 3 months or chemotherapy drugs (such as cyclophosphamide, ammonia and cancer chemotherapy) and radioactive therapy.
- Gestation or lactation period women and women who plan to get pregnant during the study period.
- Patient who are allergy to the experimental drug.
- Using history of anti-viral or anti-fibrosis drug within 6 months.
- Patients who are participating other trials.
- Other situation where PI thinks the patient should be excluded.
Key Trial Info
Start Date :
September 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2019
Estimated Enrollment :
700 Patients enrolled
Trial Details
Trial ID
NCT02241590
Start Date
September 1 2014
End Date
June 1 2019
Last Update
October 15 2018
Active Locations (20)
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1
Guangxi Ruikang Hospital
Nanning, Guangxi, China
2
The Fifth Hospital of Shijiazhuang
Shijiazhuang, Hebei, China
3
The Fifth People's Hospital of Anyang
Anyang, Henan, China
4
Jingmen No.1 People's Hospital
Jingmen, Hubei, China