We did a community-based, cluster-randomised, double-masked, placebo-controlled, 2×2 factorial trial in children aged 1–35 months. Treatment groups were placebo, iron and folic acid, zinc, and iron and folic acid with zinc, with daily doses of 12·5 mg iron, 50 μg folic acid, and 10 mg zinc. Study staff gave children tablets on 2 days each week and left tablets with caregivers for other days. All children received vitamin A supplementation twice per year. Results of the iron arm of the trial have been reported previously. Between October, 2001, and January, 2006, 41 276 children were enrolled into the placebo (n=20 308) or zinc (n=20 968) groups and were followed-up for 60 636·3 person-years. The primary outcome was child mortality, and analyses were by intention to treat. Daily reports of signs and symptoms of common morbidities in stratified random subsamples of children were assessed every week for 12 months. This study is registered at ClinicalTrials.gov, number NCT00109551.
2505 children refused to continue the trial and 3219 children were lost to follow-up. There was no significant difference in mortality between the zinc and placebo groups (316 vs 333 deaths; hazard ratio 0·92, 95 % CI 0·75–1·12). Zinc had no effect on mortality in children younger than 12 months (181 vs 168 deaths; 1·04, 0·83–1·31); mortality was lower, but not statistically significantly so, in older children receiving zinc (135 vs 165; 0·80, 0·60–1·06). The frequency and duration of diarrhoea, persistent diarrhoea, dysentery, and acute lower respiratory infections did not differ between the groups.
Total mortality of children receiving zinc supplementation was not significantly different from that of children receiving placebo. Further data are needed from other populations with endemic zinc deficiency to confirm the potential age-specific effects reported in this study.