Sharp Mary Birch Hospital for Women and Newborns
San Diego, California, 92123, United States
NCT Number: NCT04259008
Participants will be <= 32 weeks gestational age (GA) neonates randomized to parenteral nutrition (PN) prepared with standard dose trace elements or to PN prepared with standard trace elements minus manganese.
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All sexes
Interventional
Phase 4
San Diego, California, 92123, United States
Very preterm neonates <= 32+6 weeks GA receiving PN will be randomized to receive their PN prepared with standard trace elements containing 5 mcg/kg/day of manganese, or to PN prepared with no added manganese. Randomization assignment will be double masked. All participants will have whole blood manganese measurements at baseline, at 2 weeks of postnatal age, and at 8 weeks postnatal age. Because manganese is present as a contaminant in many of the ingredients used to prepare neonatal PN, this study hypothesizes that neonates randomized to no added manganese in their PN will maintain whole blood manganese concentrations above the lower limit of normal.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants randomized to the experimental intervention arm will not receive added manganese in their parenteral nutrition.
5 mCg/kg/day manganese from "Multitrace-4 Neonatal."
Time frame: Baseline
concentration of manganese in blood
Time frame: 2 weeks of age
concentration of manganese in blood
Time frame: 8 weeks of age
concentration of manganese in blood
Sharp HealthCare
Other
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