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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00197782
Other study ID # Hibboost
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date April 2003
Est. completion date December 2005

Study information

Verified date August 2018
Source Public Health England
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To measure the magnitude and persistence of the antibody response to a booster dose of Hib conjugate vaccine given between 9 months and 4 years of age to UK children who had completed primary immunisation with 3 doses of Hib vaccine given at 2/3/4 months of age either as a combined D/T/wholecellpertussis/Hib or D/T/acellularpertussis/Hib vaccine.


Recruitment information / eligibility

Status Completed
Enrollment 0
Est. completion date December 2005
Est. primary completion date December 2005
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 9 Months to 4 Years
Eligibility Inclusion Criteria:

- Written informed consent from parent or legal guardian of the infant or child

- Age >= 9 months and <4 years at recruitment

- Eligible to receive a single dose of Hib vaccine as per the UK schedule

- Receipt of three doses of Hib vaccine in infancy

Exclusion Criteria:

- History of Hib infection

- History of severe local reaction that can be confidently related to a prior Hib immunisation

- Deferral of vaccination if acute illness and/or temperature >38C on day of vaccination

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Hib conjugate vaccine


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Public Health England

References & Publications (1)

Southern J, McVernon J, Gelb D, Andrews N, Morris R, Crowley-Luke A, Goldblatt D, Miller E. Immunogenicity of a fourth dose of Haemophilus influenzae type b (Hib) conjugate vaccine and antibody persistence in young children from the United Kingdom who wer — View Citation

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