ViDES Trial (Vitamin D Extra Supplementation)

Status Recruiting

Clinical Trial Summary

The objective of the study is to compare supplementation with vitamin D at 800 IU/day to usual care for the first 28 days after birth with respect to 25 (OH) vitamin D levels and indicators of likely or plausible effects of vitamin D supplementation on the function or structure of the lung, bones, immune system, and brain in extremely premature (EP) infants who are <28 weeks gestational age (GA) or <1000 grams of birth weight (BW). The study results will be analyzed as intention to treat Bayesian analyses (Frequentist analyses will also be performed).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Vitamin D Deficiency

Clinical Trial Details

NCT number	NCT05459298
Study type	Interventional
Source	The University of Texas Health Science Center, Houston
Contact	Maria del Mar Romero López, MD
Phone	713-500-7283
Email	Maria.del.Mar.RomeroLopez@uth.tmc.edu
Status	Recruiting
Phase	N/A
Start date	September 6, 2022
Completion date	December 1, 2027

View Details

See also
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