Therapeutic Effects and Long-term Follow-up After Ending Nucleos(t)Ide Analogs Therapy in Chronic Hepatitis b

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

About this trial

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.

Eligibility criteria

Qualifiers

Patients received anti-HBV therapy with nucleos(t)ide analogs.

Last anti-HBV therapy should continue for at least 2 years.

For HBeAg positive patients, HBV DNA should keep negative for at least 1 year after HBeAg seroconversion before the therapy ending; for HBeAg negative patients, HBV DNA should keep negative for at least 2 years before the therapy ending.

Disqualifiers

Liver cirrhosis, HCC;

Patients with other factors causing active liver diseases;

Pregnancy or lactation;

Patients with HIV infection or congenital immune deficiency diseases;

Trial design

Treatments tested in this trial

  • Entecavir or Tenofovir

Treatment groups

100 Participants
are divided into 2 treatment groups