← Eichor
Study identifier: NCT07257562 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Combined Use of Bacteroides Fragilis and BCAAs on HBsAg Clearance

Condition: Chronic Hepatitis B  ·  Sponsor: First Affiliated Hospital of Fujian Medical University

PhaseN/A
Planned participants40
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this prospective observational study is to determine the effects of concomitant administration of Bacteroides fragilis and Branched-Chain Amino Acids on hepatitis B virus clearance. The primary question it aims to answer is whether this concomitant administration can promote HBV clearance. The study will observe the HBV clearance rate in chronic hepatitis B patients who receive Bacteroides fragilis and BCAA as a supplement to their routine antiviral therapy. For comparison, researchers will compare the clearance rate in this group to that observed in a control group of chronic hepatitis B patients receiving a standard antiviral regimen based on PegIFNα2b and nucleoside analogs.

This description comes directly from the study's public registry record.

Talk to the study team

JinShui Pan  ·  0086+059187981658  ·  zdy20221021@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

The First Affiliated Hospital of Fujian Medical UniversityFuzhou, Fujian, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07257562