The High Initial Dose of Monitored Vitamin D Supplementation in Preterm Infants.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age1-2
SponsorPrincess Anna Mazowiecka Hospital, Warsaw, Poland

About this trial

The aim of this study will be to assess the effectiveness of monitored vit D supplementation in a population of preterm infants and to identify whether the proper vit D supplementation in preterm infants can reduce the incidence of neonatal sepsis and incidence of metabolic bone disease.

Eligibility criteria

Qualifiers

preterm infants with a gestational age of 24+0/7 to 32+6/7 born at our clinic

preterm infants with a gestational age of 24+0/7 to 32+6/7 outborn and admitted to our intensive care unit within 48h after delivery

written informed consent form caregivers for the mother and the child to participate in the study

Disqualifiers

infants born at >32 weeks of gestation

infants with major congenital abnormalities or other severe congenital malformations

infants with genetic disorders (diagnosed before and after birth) deemed incompatible with survival

infants with diagnosed cholestasis

Trial design

Treatments tested in this trial

  • cholecalciferol/ Devikap
  • cholecalciferol/ Devikap

Treatment groups

130 Participants
are divided into 2 treatment groups

Sponsors and collaborators