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Clinical Investigation About Therapeutic Effects and Long-term Follow-up After Ending Anti-hepatitis B Virus Therapy With Nucleos(t)Ide Analogs in Patients With Chronic Hepatitis b
The study is to observe the therapeutic effects and long-term follow-up after ending anti-HBV therapy with nucleos(t)ide analogs in patients with chronic hepatitis b.
Patients with chronic hepatitis b were enrolled in the study. Age, sex, weight, height, symptoms (e.g., fatigue, poor appetite, jaundice), relapse, retreatment, occurrence of liver cirrhosis and hepatocellular carcinoma (HCC), mortality and survival rate were recorded in the study. We also observed the laboratory tests including the levels of white blood cells (WBC), red blood cells (RBC), hemoglobin (HGB), platelet (PLT), alanine transaminase (ALT), aspartate transaminase (AST), total bilirubin (TBIL), blood urea nitrogen (BUN), creatine, hepatitis B surface antigen (HBsAg), hepatitis B e antigen (HBeAg), hepatitis B virus (HBV) DNA, CD4 positive T lymphocyte (CD4+T), CD8 positive T lymphocyte (CD8+T), Type 1 helper T lymphocyte (Th1), Type 2 helper T lymphocyte (Th2),fibroscan and B ultrasound. If clinical relapse occurred, patients were retreated with nucleos(t)ide analogs.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
The Third Affiliated Hospital of Sun Yat-sen University
Guangzhou, Guangdong, China
Start Date
January 1, 2014
Primary Completion Date
December 31, 2024
Completion Date
December 31, 2024
Last Updated
November 29, 2024
100
ESTIMATED participants
Entecavir or Tenofovir
DRUG
Lead Sponsor
Third Affiliated Hospital, Sun Yat-Sen University
NCT06671093
NCT06885710
Data Source & Attribution
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View ClinicalTrials.gov Terms and ConditionsNCT06263959