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UnknownNCT03962803

Immunogenicity and Persistence of Hepatitis B Vaccination in HIV-Infected Patients

A Prospective Study on the Immunogenicity and Persistence of Hepatitis B Vaccine in HIV-Infected Patients

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Shanxi Medical University · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

At present, HIV-Infected Patients of Hepatitis B Vaccination in are vaccinated with hepatitis B vaccine according to the standard three-dose schedule immunization program, and the effect of preventing HBV infection is not ideal. This is a randomized, controlled trial. The study will evaluate the immunogenicity and persistence of 20 µg and 60 µg recombinant hepatitis B vaccine with three or four injections at months 0, 1, and 6 or 0, 1,2, and 6 in HIV-Infected Patients

Detailed description

Participants are randomized in a ratio of 1:1:1 into 20 µg recombinant hepatitis B vaccine group at months 0, 1, and 6 or 20µg recombinant hepatitis B vaccine group at months 0, 1, 2, and 6 or 60µg recombinant hepatitis B vaccine group at months 0, 1, 2, and 6. HBsAg and anti-HBs will be tested during the study period. Adverse reactions will be recorded after vaccination.

Conditions

Interventions

TypeNameDescription
BIOLOGICAL20 µg recombinant hepatitis B vaccine at months 0, 1, and 6three-dose, 20 µg per dose
BIOLOGICAL20 µg recombinant hepatitis B vaccine at months 0, 1, 2, and 6four-dose, 20 µg per dose
BIOLOGICAL60 µg recombinant hepatitis B vaccine at months 0, 1, 2, and 6four-dose, 60 µg per dose

Timeline

Start date
2019-06-05
Primary completion
2020-02-01
Completion
2023-12-01
First posted
2019-05-24
Last updated
2019-05-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03962803. Inclusion in this directory is not an endorsement.