Prevention of Myopia of Prematurity by Calcium Supplementation
Status and phase
Conditions
Treatments
Details and patient eligibility
About
The purpose of this study is to determine if supplementation of calcium by the enteral route (gut feeding) to extremely low birth weight infants will lead to less myopia (nearsightedness) at 6-12 months postnatal age.
Secondly, the study will determine if calcium supplementation is well tolerated, if it reduces the molding of these premature infants' heads, and if it decreases myopia at the 18-22 month postnatal age visit.
Full description
All infants admitted meeting the 401-1000gm birthweight and less than 14 day of age entry criteria will be screened for entry into the study. Infants may be excluded for the following: Major congenital malformations, including complex congenital heart disease (except open ductus arteriosus, atrial and ventricular septal defects), pulmonary malformations, bowel or anal stenosis or atresia, renal dysplasias, chromosomal anomalies, hydrops fetalis, bowel perforation or necrotizing enterocolitis stage 2A or greater before randomization.
Written informed consent of one parent or legal guardian must be obtained. The infants are randomized to receive unsupplemented feedings of breast milk or formula, or feedings supplemented with Ca-gluconate as outlined below.
Randomization will be stratified into the following groups: 401-750 g and 751-1000 g and performed according to a balanced block scheme with variable block size (2-6) using sealed opaque envelopes.
Total parenteral nutrition is given by nursery unit standards. Infant positioning is done by nursery unit standards.
Feeding mixtures:
Supplementation is started when enteral feeding amounts to 100 ml/kg. At that time, fortification is also introduced in infants receiving breast milk. Fortified human milk or 24 cal/oz formula, e.g. Similac Special Care 24 (SSC24), is used in all participating infants. Human milk is fortified with 1 pk Enfamil human milk fortifier per 25 ml (BMHMF).
Control group: Fortified human milk or 24 cal/oz formula. Supplemented group: Ca-gluconate powder (molar weight 430.4 g) will be measured with household measuring spoons (e.g. Rubbermaid (R)) and added to the feeding mixtures.
One eye exam will be performed at 6-12 months during routine follow-up visit. A second eye exam will be performed at 18-2 months during a follow-up visit which is part of the NICHD newborn follow-up clinic. Head measurements, specifically, front-to-back and side-to-side will be measured at randomization, 36 weeks postmenstrual age or discharge, whichever occurs first, and during the follow up visits. Urinalysis will be collected weekly.
Enrollment
Sex
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Volunteers
Inclusion criteria
- Infants with a birthweight of 401 - 1000 g and postnatal age less than 14 days
Exclusion criteria
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Major congenital malformations including
- complex congenital heart disease (except open ductus arteriosus, atrial and ventricular septal defects)
- pulmonary malformations
- bowel or anal stenosis or atresia
- renal dysplasias
- chromosomal anomalies
- hydrops fetalis
- bowel perforation or necrotizing enterocolitis stage 2A or greater before randomization.
Trial design
Primary purpose
Allocation
Interventional model
Masking
99 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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