Clinical trial
Boosting the Beneficial Non-specific Effects of Live Attenuated Vaccines: A Randomized Controlled Trial (RCT) of a Second Dose of Measles Vaccine (MV) in the Second Year of Life
Name
MV18Months
Description
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.
Trial arms
Trial start
2016-10-01
Estimated PCD
2020-05-01
Trial end
2021-05-01
Status
Completed
Treatment
Measles vaccine
Arms:
Measles vaccine
Size
3812
Primary endpoint
Mortality
30 months
Hospital admissions
30 months
Eligibility criteria
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
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'PREVENTION', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 3812, 'type': 'ACTUAL'}}
Updated at
2024-01-19
1 organization
1 product
2 indications
Organization
Bandim Health ProjectProduct
Measles vaccineIndication
Child MortalityIndication
Child Morbidity