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Bacillus Calmette-Guerin (BCG) Vaccine and Morbidity From Malaria
This study has been completed.
Sponsors and Collaborators: Gates Malaria Partnership
Bandim Health Project
Hospital Nacional Simao Mendes, Bissau
Statens Serum Institut, Copenhagen, Denmark
London School of Hygiene and Tropical Medicine
Information provided by: Gates Malaria Partnership
ClinicalTrials.gov Identifier: NCT00131794
  Purpose

BCG vaccine is given at or shortly after birth in many developing countries to prevent tuberculosis. In Guinea Bissau, it has been shown that its protective effect against death is greater than would be expected from its effect against tuberculosis. This observation suggests that BCG may enhance the ability of the immune system of young children to make a protective response to other infections, including malaria. There is some evidence to support this hypothesis as BCG protects against malaria in experimental animals.

Because BCG is a recommended vaccine, a randomised controlled trial of BCG at birth would not be ethically justifiable. However, it is not known whether re-vaccination with BCG in the second year of life might provide some added benefit and a large study to determine this is under way in Guinea Bissau. This study examined the effect of re-vaccination with BCG on the incidence of clinical malaria. If re-vaccination with BCG at 19 months of age is found to protect against malaria this would support the hypothesis that one of the ways that BCG at birth provides protection to young children is through an effect on malaria.


Condition Intervention Phase
Malaria
Biological: BCG
Phase III

MedlinePlus related topics: Malaria
Drug Information available for: BCG Vaccine
U.S. FDA Resources
Study Type: Interventional
Study Design: Prevention, Randomized, Single Blind, Placebo Control, Single Group Assignment, Efficacy Study
Official Title: The Effect of BCG Vaccine on Morbidity From Malaria

Further study details as provided by Gates Malaria Partnership:

Primary Outcome Measures:
  • Incidence of clinical malaria.

Secondary Outcome Measures:
  • Prevalence of malaria parasitemia.

Estimated Enrollment: 1200
Study Start Date: January 2003
Estimated Study Completion Date: December 2003
  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Months to 24 Months
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Age more than 18 months and less than 24 months
  • Previous BCG vaccination

Exclusion Criteria:

  • Mantoux skin reaction > 14 mm
  • Chronic underlying illness
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00131794

Locations
Guinea-Bissau
Bandim Health Project
Bissau, Guinea-Bissau, 1004 Bissau CODEX
Sponsors and Collaborators
Gates Malaria Partnership
Bandim Health Project
Hospital Nacional Simao Mendes, Bissau
Statens Serum Institut, Copenhagen, Denmark
London School of Hygiene and Tropical Medicine
Investigators
Principal Investigator: Amabelia Rodrigues, PhD Bandim Health Centre, Bissau.
  More Information

Gates Malaria partnership web site  This link exits the ClinicalTrials.gov site

Study ID Numbers: ITDCVG31
Study First Received: August 18, 2005
Last Updated: October 13, 2005
ClinicalTrials.gov Identifier: NCT00131794  
Health Authority: Guinea-Bissau: Ministry of Health

Keywords provided by Gates Malaria Partnership:
Malaria
BCG vaccine
Guinea Bissau

Study placed in the following topic categories:
BCG Vaccine
Protozoan Infections
Parasitic Diseases
Malaria

Additional relevant MeSH terms:
Coccidiosis

ClinicalTrials.gov processed this record on January 16, 2009