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Immunological response after early extra and regular MMR immunization; 6 years follow-up

Completed
Conditions
Measles infection
paramyxovirus
10047438
Registration Number
NL-OMON48447
Lead Sponsor
RIVM
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
90
Inclusion Criteria

•Previous participation in the study on the immunological effects of early measles vaccination, as described in a separate study protocol (NL45616.094.13/IIV-273)
•The parents/legally representatives accept participation in the trial according to the described procedures
•Presence of a signed informed consent
•Children must have received their NIP vaccinations according to schedule.

Exclusion Criteria

•Receiving immunosuppressive medication
•Presence of a serious disease that requires medical care that can interfere with the results of the study
•Known or suspected immunological disorder
•Bleeding disorders

Study & Design

Study Type
Observational invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>• Measles specific serum neutralizing antibodies 6 years after MMR-1 at 14<br /><br>months of age </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>• Measles specific serum IgG antibody and avidity (Luminex), and functional<br /><br>antibody characteristics prior 6 years after MMR-1 at 14 months of age<br /><br>• Serum IgG antibody concentrations against mumps and rubella (Luminex) 6 years<br /><br>after MMR-1 at 14 months of age<br /><br>• Antibodies against other NIP vaccines 6 years after MMR-1 at 14 months of age </p><br>
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