Nucleoside (Acid) Analogues Treatment in Patients With Normal ALT and Positive HBVDNA.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorThird Affiliated Hospital, Sun Yat-Sen University

About this trial

This study is to investigate the clinical efficacy and safety of Nucleoside (acid) analogues treatment in patients with normal Alanine Aminotransferase and positive Hepatitis B virus DNA.

Eligibility criteria

Qualifiers

Positive hepatitis b surface antigen and hepatitis b antibody > 0.5 year;

Age from 18 to 65 years old;

Serum Alanine Aminotransferase(ALT) ≤1×ULN at least 12 weeks;

Positive Hepatitis b virus(HBV);

Disqualifiers

Other active liver diseases;

Hepatocellular carcinoma or other malignancy;

Pregnancy or lactation;

Human immunodeficiency virus infection or congenital immune deficiency diseases; 5.Severe diabetes, autoimmune diseases; 6.Other important organ dysfunctions; 7.Using glucocorticoid; 8.Patients can not follow-up; 9.Investigator considering inappropriate.

Trial design

Treatments tested in this trial

  • Tenofovir alafenamide Fumarate

Treatment groups

200 Participants
are divided into 2 treatment groups