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Active Not Recruiting
NCT05459298
ViDES Trial (Vitamin D Extra Supplementation)
Conditions: Vitamin D Deficiency
Sex: All
Ages: 24 Hours – 96 Hours
Healthy volunteers: No
Phase: NA
Enrollment: 180
Sponsor: The University of Texas Health Science Center, Houston
Location: The University of Texas Health Science Center at Houston Houston Texas
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 \
Eligibility Criteria
Inclusion Criteria:
* Infants born at \< 28 weeks gestational age (GA) or \32 weeks regardless of birth weight (BW)
* Any major congenital anomaly
* A known congenital nonbacterial infection
* Prenatal diagnosis of disorders that affect vitamin D absorption (e.g, cystic fibrosis)
* Such severe illness or immaturity that the attending neonatologist judges intensive care to be unjustified.
Source: ClinicalTrials.gov (NCT05459298). StuddyBuddy aggregates publicly available trial information.
