Chronic Hepatitis b Clinical Trial
Official title:
Evaluation of Antiviral Indications and Therapeutic Effect by Liver Biopsy Combined With Clinical Trial Parameters on Chronic HBV Infection With Different Transaminase Levels
Verified date | August 2018 |
Source | First Affiliated Hospital Xi'an Jiaotong University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
It remains unknown whether antiviral therapy is beneficial for chronic hepatitis B (CHB) with normal or mild ALT.The investigators aim to evaluate the antiviral indications combining liver biopsy and clinical parameters,and further clarify the response indexes of clinical results such as virological, serological, biochemical and histological responses from a retrospective observational cohort study on antiviral therapy in HBeAg positive and negative patients with different ALT levels,especially when ALT lower 2 times upper limit of normal (ULN).
Status | Active, not recruiting |
Enrollment | 700 |
Est. completion date | June 2019 |
Est. primary completion date | April 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 70 Years |
Eligibility |
Inclusion Criteria:All of below 1. Patients with chronic HBV infection,defined as those in whom presence of serum hepatitis B surface(HBsAg) for more than 6 months; 2. All patients had underwent a liver biopsy; 3. All patients signed the informed consent before liver biopsy; 4. No history use of interferon or Nucleoside analogue treatment. Exclusion Criteria:Any of below 1. Co-infection with hepatitis A virus(HAV),hepatitis C virus(HCV),hepatitis D virus(HDV) hepatitis E virus(HEV) and/or human immunodeficiency virus(HIV); 2. Decompensated cirrhosis; 3. History of hepatocellular carcinoma(HCC); 4. History of liver transplantation; 5. Patient with a history of antiviral treatment; 6. Patient has medical condition that requires concurrent use of systemic prednisolone or other immunosuppressive agent (including chemotherapeutic agent) 7. Patient has one or more additional known primary or secondary causes of liver disease, other than hepatitis B (e.g., alcoholism, autoimmune hepatitis, malignancy with hepatic involvement, hemochromatosis,alpha-1 antitrypsin deficiency, Wilson's Disease, other congenital or metabolic conditions affecting the liver, congestive heart failure or other severe cardiopulmonary disease, etc.) 8. Patient who interrupted antiviral therapy; 9. Patient with incomplete data; 10. Follow up less than 1 year. |
Country | Name | City | State |
---|---|---|---|
China | The Affiliated Hospital of Yan'an University | Yanan | Shaanxi |
Lead Sponsor | Collaborator |
---|---|
First Affiliated Hospital Xi'an Jiaotong University | The Affiliated Hospital of Yan’an University |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Virological response in patients with different ALT levels | Serum HBV DNA will be summarized and compared between different groups at baseline and follow-up endpoint | at 1 year | |
Secondary | Changes in serum HBsAg, HBeAg ,HBeAb ,HBcAb levels between treated and untreated groups | at baseline and 1 year | ||
Secondary | Proportion of patients with normal alanine aminotransferase(ALT) between treated and untreated groups | at baseline and 1 year | ||
Secondary | Liver stiffness measurement(LSM) changes between treated and untreated groups | LSM response is defined as LSM decrease at least a 1-kilopascal | at baseline and 1 year | |
Secondary | Proportion of patients with HBsAg loss or seroconversion | at 1 year | ||
Secondary | (5) Predictive values of HBV DNA,HBsAg and LSM for the antiviral indications of chronic HBV infection with different ALT levels | at baseline |
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