Malnutrition Clinical Trial
Official title:
LCNI-6. A Single-centre Intervention Trial in Rural Malawi, Testing the Efficacy of Fortified Spread or Maize-soy Flour Supplementation to Alleviate Moderate Malnutrition Among 6-18 Month Old Children
This study tests the hypothesis that moderately underweight but not severely wasted 6-17-month old infants receiving fortified spread or maize-soy flour as a food supplement for 12 weeks grow better during the supplementation than infants who do not get any food supplement.
Status | Completed |
Enrollment | 189 |
Est. completion date | July 2007 |
Est. primary completion date | July 2007 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 6 Months to 15 Months |
Eligibility |
Inclusion Criteria: - signed informed consent from at least one guardian - age 6.00 months to 14.99 months - weight-for-age <-2.0 Z scores - availability during the period of the study. - permanent resident Lungwena Health Centre catchment area Exclusion Criteria: - moderate or severe wasting (WHM<80% of the reference median) - history of peanut allergy - history of any serious allergic reaction to any substance, requiring emergency medical care - history of anaphylaxis - severe illness warranting hospital referral - concurrent participation in another clinical trial with intervention to the child |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Malawi | College of Medicine, University of Malawi | Mangochi | Mangochi District |
Lead Sponsor | Collaborator |
---|---|
University of Tampere | University of Malawi College of Medicine |
Malawi,
Thakwalakwa C, Ashorn P, Phuka J, Cheung YB, Briend A, Puumalainen T, Maleta K. A lipid-based nutrient supplement but not corn-soy blend modestly increases weight gain among 6- to 18-month-old moderately underweight children in rural Malawi. J Nutr. 2010 — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Weight gain during the 12-week follow-up (in grams) | |||
Secondary | Length gain during the 12-week follow-up (in centimetres) | |||
Secondary | Change in blood haemoglobin concentration during the study period (g/l) | |||
Secondary | Change in serum ferritin concentration during the study period (µg/l) | |||
Secondary | Change in anthropometric indices (WAZ, WHZ and HAZ) | |||
Secondary | Proportion developing moderate or severe wasting during the intervention (WHM<80% of the reference median) | |||
Secondary | Change in mid-upper arm and head circumference |
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