EligibleTrials

Real-world Study Optimizing Nucleotide-analogues

Recruiting · NCT05937178 · Observational (researchers observe without assigning treatment) · Lead sponsor: Huashan Hospital

View the official record on ClinicalTrials.gov →
Hepatitis B

Interventions studied

ETV/TAF/TDF/TMFETV/TAF/TDF/TMF/IFN

What this trial is about

The goal of this multicenter, observational, prospective study is to observe and compare different anti-viral treatment strategies in a real-world cohort of patients with CHB managed in routine clinical settings in China. The main questions it aims to answer are: 1. To evaluate the benefits of initiating first-line nucleos(t)ide analogue in patients with chronic HBV infection who are recommended in the updated Chinese Guideline 2022, but not recommended in the Chinese Guideline 2019. 2. To evaluate the Chinese Guideline recommends initiation of treatment, but at least one foreign authoritative guideline (eg. AASLD, EASL) does not recommend the benefit of initiating first-line nucleos(t)ide analogue in patients with chronic HBV infection who initiate treatment. 3. To compare the treatment effect of different alternatives with patients who have partial response after treatment with first-line nucleos(t)ide analogues.

Who can take part

Age range
18 Years to 80 Years
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)

Inclusion criteria

Exclusion criteria

Where it is running

44 locations listed.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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