mumps
Conditions
Interventions
None listed
Sponsors
Leids Universitair Medisch Centrum
Eligibility
Age
18 Years to 99 Years
Inclusion criteria
Inclusion criteria: Medical students (2nd, 3rd, 4th year) from the LUMC.
Exclusion criteria
Exclusion criteria: No exclusion.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| In the first analysis, the primary study parameter will be the measured mumps titers in the paired serumsamples in the group that has claimed to have had a clinical mumps infection. As a controle on the natural behaviour of MMR antibody titers after several years, also measles and rubella titers will be measured in the same multiplex ELISA at the RIVM. In a second analysis, the occurence of clinical mumps (based on the questionnaire) and subclinical mumps (based on a similar titerrise as in the group with clinical mumps) is the primary study parameter. In this case, the effect of the mumpstiters on the occurence of mumps will be investigated. | — |
Secondary
| Measure | Time frame |
|---|---|
| As secondary parameters the relation between the number of MMR vaccines (0, 1 of 2) will be related to the mumpstiters in the first serum sample. | — |
Countries
Netherlands
Outcome results
None listed