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Randomized Controlled Trial
. 2007 May;85(5):1312-9.
doi: 10.1093/ajcn/85.5.1312.

Randomized controlled safety and efficacy trial of 2 vitamin A supplementation schedules in Tanzanian infants

Boniphace Idindili  1 , Honarati Masanja, Honorathy Urassa, Wilbert Bunini, Paul van Jaarsveld, John J Aponte, Elizeus Kahigwa, Hassan Mshinda, David Ross, David M Schellenberg
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Free article
Randomized Controlled Trial

Randomized controlled safety and efficacy trial of 2 vitamin A supplementation schedules in Tanzanian infants

Boniphace Idindili et al. Am J Clin Nutr. 2007 May.
Free article

Abstract

Background: Vitamin A supplementation reduces morbidity and mortality in children living in areas endemic for vitamin A deficiency. Routine vitamin A supplementation usually starts only at age 9 mo, but high rates of illness and mortality are seen in the first months of life.

Objective: The objective of the study was to evaluate the safety and efficacy of vitamin A supplementation at the same time as routine vaccination in infants aged 1-3 mo.

Design: We recruited 780 newborn infants and their mothers to a randomized double-blind controlled trial in Ifakara in southern Tanzania. In one group, mothers received 60,000 microg vitamin A palmitate shortly after delivery, and their infants received 7500 microg at the same time as vaccinations given at approximately 1, 2, and 3 mo of age. In the other group, mothers received a second 60,000-microg dose when their infant was aged 1 mo, and their infants received 15,000 microg at the same time as the routine vaccinations. VAD was defined as a modified relative dose-response test result of >or=0.060.

Results: High-dose vitamin A supplementation was well tolerated. The relative risk of VAD at 6 mo in the high-dose group compared with the lower dose group was 0.91 (95% CI: 0.76, 1.09; P=0.32). Serum retinol and incidence of illness did not differ significantly between the 2 groups. Some vitamin A capsules degraded toward the end of the study.

Conclusions: Doubling the doses of vitamin A to mothers and their young infants is safe but unlikely to reduce short-term morbidity or to substantially enhance the biochemical vitamin A status of infants at age 6 mo. The stability of vitamin A capsules merits further investigation.

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