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NCT Number: NCT04970836

The Immune Responses After Hepatitis B Revaccination Doses in a Young Cohort

This prospective cohort study aims to provide the evidence-based clinical guide to help decide the revaccination doses of hepatitis B vaccine that the high-risk young adults without hepatitis B seroprotective antibodies (anti-HBs titer<10 mIU/mL) need to take.

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Key information

Age range

20 year–36 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Family Medicine, NTUH

Taipei, 100, Taiwan

Location status: Recruiting

Location contact

CHYI-FENG JAN, MD, PhD

CONTACT

[email protected]

+886-2-23123456 ext. 66824

About this study

Purpose For young adults born after the neonatal hepatitis B immunization program, especially those who were 20-33 years old after 1987, additional hepatitis B vaccination may have the benefit of strengthening protection from acute hepatitis B infection among high-risk groups. However, how many doses are most appropriate for the protection of high-risk groups is still an issue to be resolved. This study aims to provide the evidence-based clinical guide to help decide the revaccination doses of hepatitis B vaccine that the high-risk young adults without hepatitis B seroprotective antibodies (anti-HBs titer<10 mIU/mL) need to take.

Materials and Methods From August 2021 to July 2024, the investigator will invite young adults born in Taiwan over the age of 20 and born after 1987, who have received a full course of hepatitis B vaccine at least three doses at their infant period. Those who are all negative for hepatitis B surface antibodies (anti-HBs) and surface antigens (HBsAg) are enrolled to 4 groups according to the anti-HBs titer concentration (anti-HBs titer between 2.5-10 mIU/mL is a low concentration, anti-HB titer less than 2.5 mIU/mL is an extreme low concentration) with one or two doses of hepatitis B vaccine (Engerix-B) administered, respectively. Each group recruits 60 cases to reach a total of 240 participants. Each participant was followed for 12 months, and the anti-HBs titer concentration was measured in 0, 7-10 days, 28 days, 24- 28 weeks, and 48-52 weeks. The investigator will calculate the anti-HBs titer reaction rate and immune response after receiving hepatitis B vaccine(s) at each stage, and do further univariate and multivariate analysis.

Expected Results This prospective cohort study can help understand the difference in the anti-HBs titer response after 1 or 2 revaccination doses by the anti-HBs titer concentration as well as the two different types of hepatitis B vaccination in childhood It is expected to provide an important reference for the administration of hepatitis B vaccine in young adults of high-risk groups.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • The actual age at the time of admission was higher than 20 years old and birth year after 1987
  • Born in Taiwan and had received a full course of hepatitis B vaccines at least three doses at infant period.
  • Those who have tested negative for hepatitis B surface antibody and surface antigen at baseline
  • Have never been vaccinated against hepatitis B in childhood and adolescence by questionnaire
  • Consent to administer 1-2 doses of hepatitis B vaccine according to the assigned group after sharing decision making process
  • In good health

Exclusion criteria

  • Those who were previously allergic to hepatitis B vaccine or its components (such as yeast)
  • Those who have been vaccinated against hepatitis B during childhood and adolescence
  • Those who have a positive test for hepatitis B surface antibody or a positive test for hepatitis B surface antigen

Treatment and study plan

recombinant hepatitis B vaccine

Biological

Hepatitis B vaccine (Engerix-B) will be administered to the eligible participants by 4 groups. Each case will be tracked for 12 months, at 0, 7-10 days, 28 days, 24-28 weeks, 48-52 weeks anti-HBs titer concentration and 4 follow-up questionnaires.

Other names: Engerix-B

Primary outcomes

  1. anti-HBs titer response rate at 7-10 days

    Time frame: 7-10 days

    the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)

  2. anti-HBs titer response rate at one month

    Time frame: 28 days

    the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)

  3. anti-HBs titer response rate at 6 months

    Time frame: 24-28 weeks

    the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)

  4. anti-HBs titer response rate at 12 months

    Time frame: 48-52 weeks

    the anti-HBs titer response rate after 1-2 doses of hepatitis B vaccine(s)

  5. anti-HBs titer immune response change at 12 months

    Time frame: 48-52 weeks

    anti-HBs titer immune response change at 12 months after 1-2 doses of hepatitis B vaccine(s)

Study contacts

Contact information is provided by the study sponsor or research team.

CHYI-FENG JAN, MD, PHD

CONTACT

[email protected]

+886-2-23123456 ext. 66824

Sponsors and collaborators

Lead sponsor

National Taiwan University Hospital

Other

Collaborators

  • Academia Sinica, Taiwan
  • Ministry of Science and Technology, Taiwan

Registry information

Acronym: IRHBRVD

Important dates

Study start
2021
Primary completion
2027
Study completion
2027
First posted
Jul 21, 2021
Registry last updated
Mar 20, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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