Bandim Health Project, Apartado 861
Bissau, Guinea-Bissau
NCT Number: NCT00244673
In non-randomized studies, routine childhood vaccinations have been observed to have non-targeted effects. Difteria-tetanus-pertussis (DTP) vaccine provided with or after measles vaccine (MV) is associated with increased mortality in areas with herd immunity to pertussis.
We will examine in a randomised study of 6000 children the effect of not administering DTP simultaneously with or after MV on overall child mortality, hospitalization rates, and the immunological responses after vaccination. We will also examine potential sex-differential effects in the outcomes and interactions with other vaccines, other health interventions and season.
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Notify Me9 month–4 year
All sexes
Interventional
Phase 4
Bissau, Guinea-Bissau
Background: Infectious diseases are the main cause of high child mortality in Africa. In several non-randomised studies, routine childhood vaccinations have been observed to have non-targeted effects. Live vaccines like measles vaccine (MV) seem to protect against overall mortality, whereas killed vaccines, like DTP, may have no beneficial effects, especially for girls. DTP provided with or after MV may be associated with increased mortality. The mechanisms behind these effects are unknown.
Hypothesis: Not providing DTP together with or after MV is associated with a 35 % reduction in overall mortality and 23% reduction in hospitalizations.
Objectives: To examine in a randomised study of 6000 children the effect of not administering DTP simultaneously with or after MV on
Methods:
Surveillance system: BHP's demographic surveillance system in Bissau covers 6 districts with a population of 90,000; 3,500 children are born each year.
Hospitalizations: There is only one pediatric ward in Bissau and all hospitalizations are identified in the BHP register.
Vaccinations: Vaccinations are provided and registered at the 3 health centres in the study area.
Intervention: In this study 6000 children are randomised as they come to receive DTP3 or DTP booster with or after measles vaccination (MV) at the local health centres. Children will be randomised to DTP3+OPV3 and MV versus OPV3 and MV or DTP4+OPV4 versus OPV4 (booster doses).
Follow-up: The children will be followed until 4 years of age or end of study.
Sample size: With a total of 7500 person-years of follow-up, we will be able to document a 35% reduction in mortality and a 23% reduction in hospitalizations. A subgroup of children will be examined for possible differences in immunological profile after vaccination.
Ethical considerations: Herd immunity to pertussis should not be affected as, due to the intervention, more children is vaccinated.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Normally applied contraindications for receiving vaccinations, including high fever
Trial of not providing 3. and/or 4. DTP together with or after MV at 9 to 18 month of age.
Time frame: June 2011
Time frame: June 2011
Time frame: December 2008
Time frame: July 2008
Time frame: June 2011
Bandim Health Project
Other
Diphteria-tetanus-pertussis (DTP) Vaccination and Child Survival: Randomized Study of Not Providing DTP Vaccination Together With or After Measles Vaccination
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