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Exploratory study into age-related immunological differences related to immunogenicity in influenza vaccination and herpes zoster vaccination

Exploratory study into age-related immunological differences related to immunogenicity in influenza vaccination and herpes zoster vaccination - INFLUENZA-SHINGRIX

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON50860
Enrollment
140
Registered
2021-01-05
Start date
2021-09-20
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

herpes zoster Influenza

Interventions

There are several interventions: The older adults will receive either the influenza vaccine or the herpes zoster vaccine Young adults will receive either the influenza vaccine, the herpes zoster vac

Sponsors

Radboud Universitair Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • Healthy • Age between 18-35 years old OR age >=65 years old • Written informed consent

Exclusion criteria

Exclusion criteria: • Known allergy to (components of) the influenza or herpes zoster vaccine • Immunocompromised subjects • Previous herpes zoster vaccination in the last year • Receipt of any vaccination 4 weeks prior to the start of the study or plans to receive any other vaccination until 2 months after inclusion • Chronic use of systemic drugs other than oral contraceptives • Use of NSAIDS less than 4 weeks prior to the start of the study • Acute or active illness within two weeks prior to the start of the study • Pregnant, breastfeeding or planning to become pregnant during the study period

Design outcomes

Primary

MeasureTime frame
Functional assessment of vaccine response (including but not limited to antibody responses, cellular mediated immune responses, cross-omics, cytokine production)

Secondary

MeasureTime frame
Safety data (solicited AEs, unsolicited AEs, SAEs, MAAEs, AESIs, AEs leading to withdrawal from the study and unintentional exposure during pregnancy)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)