MATERIAL AND METHODS: We searched several databases using Cochrane Central Register of Controlled Trials, MEDLINE, Embase, and ClinicalTrials.gov. We included only placebo-controlled clinical trials on infants born at less than 32 weeks' gestation, who were administered enteral vitamin A supplementation. A random effects model was employed to calculate risk ratios and weighted mean differences. RESULTS: A total of five studies with 1715 participants were included in our meta-analysis. No significant reduction was observed in the incidence of moderate-to-severe bronchopulmonary dysplasia [RR = 0.91, 95% CI (0.70, 1.17), = 0.45], retinopathy of prematurity requiring treatment [RR = 0.94, 95% CI (0.62 to 1.42), = 0.76], sepsis [RR = 0.96 95% CI (0.74 to 1.24), = 0.73], mortality RR = 0.86, 95% CI, (0.65 to 1.15), = 0.31], and duration of mechanical ventilation [MD = -0.93 days 95% CI (-2.90 to 1.04) = 0.36] between the vitamin A and control group. Among the secondary outcomes, only the duration of CPAP/HFNC (days) showed statistically significant results [MD = -1.29, 95%CI (-1.93, -0.66), < 0.0001]. Meanwhile, there was no statistically significant difference between the experimental and placebo groups with regards to duration of hospitalization, duration of minimally invasive ventilation and oxygen, requirement for postnatal steroids, serum retinol concentration at 28 days, necrotizing enterocolitis, periventricular leukomalacia, intraventricular hemorrhage and vomiting. CONCLUSION: Supplementing premature infants with enteral vitamin A might shorten the duration of noninvasive respiratory support requirement. However, there is a lack of evidence for its superior efficacy in improving the overall health outcomes for premature infants compared to placebo.