Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02943681
Other study ID # MV18Months
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date May 2021

Study information

Verified date January 2024
Source Bandim Health Project
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 3812
Est. completion date May 2021
Est. primary completion date May 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Months to 24 Months
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Measles vaccine


Locations

Country Name City State
Guinea-Bissau Bandim Health Project, Apartado 861 Bissau

Sponsors (1)

Lead Sponsor Collaborator
Bandim Health Project

Country where clinical trial is conducted

Guinea-Bissau, 

References & Publications (1)

Berendsen MLT, Silva I, Bale C, Nielsen S, Hvidt S, Martins CL, Benn CS, Aaby P. The Effect of a Second Dose of Measles Vaccine at 18 Months of Age on Nonaccidental Deaths and Hospital Admissions in Guinea-Bissau: Interim Analysis of a Randomized Controlled Trial. Clin Infect Dis. 2022 Oct 12;75(8):1370-1378. doi: 10.1093/cid/ciac155. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Mortality Mortality registered monthly by Health and Demographic Surveillance System fieldworkers. Mortality will be combined with hospital admissions in the analysis to form the outcome severe morbidity. This will be examined overall and by sex 30 months
Primary Hospital admissions Hospital admissions registered daily at the national hospital. Hospital admissions will be combined with mortality in the analysis to form the outcome severe morbidity. This will be examined overall and by sex 30 months
Secondary Hospital admission by cause Causes of hospital admissions registered daily at the national hospital. These will be examined overall and by sex 30 months
Secondary Consultations Consultations registered daily at the local health centers and the national hospital. These will be examined overall and by sex 30 months
See also
  Status Clinical Trial Phase
Recruiting NCT04716712 - Infant Mortality Reduction by the Mass Administration of Azithromycin Phase 4
Completed NCT02233127 - Birth Cohort in Rahimyar Khan, Pakistan N/A
Completed NCT03676751 - MORDOR II Burkina Faso: Longitudinal Trial Phase 4
Completed NCT04617626 - Resiliency Through Azithromycin for Children (REACH), Côte d'Ivoire N/A
Completed NCT03367832 - South African Paediatric Surgical Outcomes Study (SAPSOS) N/A
Recruiting NCT00656591 - Community-Based Interventions for Infant Health in Nepal Phase 1
Recruiting NCT04235816 - Improving Care Through Azithromycin Research for Infants in Africa Phase 3
Recruiting NCT05016895 - REACH2: Implementation Research on Bi-Annual Mass Distribution of Azithromycin to Children 1-11 Months in Côte d'Ivoire N/A
Completed NCT01571765 - MNCH Programming in Southwest Uganda Maternal and Child Health In Bushenyi and Rubirizi Districts, UGANDA N/A