Malaria Clinical Trial
Official title:
Evaluation of the Impact of Vitamin A and Zinc Supplementation on Malarial Morbidity in Ghana
Verified date | January 2013 |
Source | Kintampo Health Research Centre, Ghana |
Contact | n/a |
Is FDA regulated | No |
Health authority | Ghana : Food and Drugs Board |
Study type | Interventional |
The purpose of this study was to determine whether young children receiving Vitamin A and Zinc supplements will have a lower incidence of symptomatic malaria than similar children receiving vitamin A supplements alone.
Status | Completed |
Enrollment | 200 |
Est. completion date | November 2009 |
Est. primary completion date | November 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 6 Months to 24 Months |
Eligibility |
Inclusion Criteria: - Children aged 6 - 24 months - Child's guardian is willing to provide informed consent - Child's family plans to remain resident in the study areas during the study period Exclusion Criteria: - Clinical evidence of vitamin A deficiency - Severe acute malnutrition - Severe illness - Child aged <6 months or >24 months - Receipt of vitamin A supplement within the last three months |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Ghana | Kintampo Health Research Centre | Kintampo | Brong Ahafo |
Lead Sponsor | Collaborator |
---|---|
Kintampo Health Research Centre, Ghana | International Atomic Energy Agency, University of Wisconsin, Madison |
Ghana,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | incidence of clinical malaria attacks | 6 months | No | |
Secondary | changes in weight and height/length | Enrollment and end of supplementation | baseline and 6 months | No |
Secondary | changes in vitamin A and zinc nutritional status within and between the groups | enrollment and end of supplementation | baseline and 6 months | No |
Secondary | change in prevalence of anemia | enrollment and end of supplementation | baseline and 6 months | No |
Secondary | the incidence of diarrhea and pneumonia | 1 time/week, enrollment to end, total:24 | 1 time per week up to 6 months | No |
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