drugset / Trial / NCT01203488

Vitamin A Supplementation for Extremely-Low-Birth-Weight Infants

NCT01203488

RandomizedParallel-groupTriple-blindPrevention

Summary

This multi-site, randomized trial was conducted to determine the safety and effectiveness of a higher dose of vitamin A and determine if this would increase the rate of survival without bronchopulmonary dysplasia (BPD) and reduce the risk of sepsis. Infants with birth weights from 401-1000g and who were on mechanical ventilation or supplemental oxygen at 24-96 hours of age were enrolled. Subjects were randomized to either the Vitamin A or a control group. Infants in the Vitamin A group were given a dose of 5000 IU (0.1 ml) intramuscularly on Mondays, Wednesdays, and Fridays for four weeks. Control infants received a sham procedure rather than placebo injections.

Timeline

Start
1996-01
Primary completion
1997-07
Completion
1999-07

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Vitamin A Unknown 5000 iu Intramuscular