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RECRUITINGOBSERVATIONAL

Immune Responses in Health Care Personnel

Immune Responses to Influenza Vaccinations and Viruses Among Health Care Personnel

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This is an investigator-initiated 10 year long open cohort observational study, aiming to increase the understanding of the humoral and cellular immunological mechanisms of vaccination against influenza, including effects of repeated vaccination, the duration of protection, immunity against circulating viruses, as well as factors affecting the immunological responses and immunity against other vaccine preventable infectious diseases among health care personnel.

Who May Be Eligible (Plain English)

Who May Qualify: - Members of health care or laboratory personnel in HUS having decided to take the seasonal influenza vaccination by the routine occupational health care service - General good health as established by or volunteer's own statement - Written willing to sign a consent form - Presumably able and willing to participate in the study during the starting influenza season Who Should NOT Join This Trial: - Any confirmed or suspected immunosuppressive or immunodeficient condition, including human weakened immune system virus (HIV) infection. - Administration (longer than 14 days) of immunosuppressants or other immune- modifying drugs within 6 months before the vaccination; oral corticosteroids in dosages of 20 mg/day or more prednisolone or equivalent are excluded; inhaled or topical steroids are allowed. - Pregnancy or lactation - Acute disease at the time of enrolment (defined as the presence of a moderate or severe illness with or without fever) - Contraindication for influenza vaccination - Any other criteria which, in the investigator's or dedicated study staff member's opinion, would compromise the ability of a subject to participate in the study, a subject's well-being, or the outcome of the study Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Members of health care or laboratory personnel in HUS having decided to take the seasonal influenza vaccination by the routine occupational health care service * General good health as established by or volunteer's own statement * Written informed consent * Presumably able and willing to participate in the study during the starting influenza season Exclusion Criteria: * Any confirmed or suspected immunosuppressive or immunodeficient condition, including human immunodeficiency virus (HIV) infection. * Administration (longer than 14 days) of immunosuppressants or other immune- modifying drugs within 6 months before the vaccination; oral corticosteroids in dosages of 20 mg/day or more prednisolone or equivalent are excluded; inhaled or topical steroids are allowed. * Pregnancy or lactation * Acute disease at the time of enrolment (defined as the presence of a moderate or severe illness with or without fever) * Contraindication for influenza vaccination * Any other criteria which, in the investigator's or dedicated study staff member's opinion, would compromise the ability of a subject to participate in the study, a subject's well-being, or the outcome of the study

Treatments Being Tested

BIOLOGICAL

influenza vaccine

Vaccine for prevention of influenza. Vaccines change by influenza season.

Locations (1)

The Hospital District of Helsinki and Uusimaa
Helsinki, Finland