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A Second Dose of Measles Vaccine (MV) in the Second Year of Life

B

Bandim Health Project

Status

Completed

Conditions

Child Morbidity
Child Mortality

Treatments

Biological: Measles vaccine

Study type

Interventional

Funder types

Other

Identifiers

NCT02943681
MV18Months

Details and patient eligibility

About

This study evaluates the non-specific effects on child mortality and morbidity of a second dose of measles in the second year of life. Half of the study participants will receive a second dose of measles vaccine at 18 months of age while the other half will receive a second dose of measles by 4 years of age or at the end of the study.

Enrollment

3,812 patients

Sex

All

Ages

18 to 24 months old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Children need to have received the third dose of inactivated vaccines (Penta, PCV13 and IPV) before measles vaccination.

Exclusion criteria

  • Having severe malformations that impairs their health
  • Having received a second dose of measles vaccine
  • Severely ill (requiring hospitalization) upon clinical examination

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

3,812 participants in 2 patient groups

Measles vaccine
Experimental group
Description:
Measles vaccine, 1 dose of 0.5 ml
Treatment:
Biological: Measles vaccine
Control
No Intervention group
Description:
Nothing

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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