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SARS-CoV-2 vaccination response in people living with HIV

Conditions
COVID-19, HIV
Registration Number
NL-OMON26993
Lead Sponsor
OLVG, LUMC, Erasmus MC
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
1000
Inclusion Criteria

18 years or older, confirmed HIV-infection, selected by national regulations for SARS-CoV-2 vaccination

Exclusion Criteria

none

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To determine the humoral vaccine efficacy against SARS-CoV-2 in PLWHIV 2 weeks after the completed vaccination schedule (all participants)
Secondary Outcome Measures
NameTimeMethod
1. To find factors associated with intensity of immune response and/or related adverse events (all participants)<br>2. To determine the humoral vaccine efficacy against SARS-CoV-2 in PLWHIV 3 weeks after the first vaccination (subgroup participants)<br>3. To measure anti-SARS-CoV-2 neutralising antibody response (subgroup participants)<br>4. To determine the duration of serologic anti-SARS-CoV-2 immune responses over time (all participants)<br>5. To evaluate anti-SARS-CoV-2 specific T-cell responses (subgroup participants)
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