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Prevention as prevention of Neonatal Hypoglycaemia, sponsored by University of Auckland

Get in touch This trial recruits from July 2013 for 35 weeks

Prof Jane Harding

Phone: +64 9 3737599 ext 85872

Email: j.harding@auckland.ac.nz

Address:
Liggins Institute
2-6 Park Avenue,
Private Bag 92019
Auckland 1142

Inclusion Criteria

Gender: Both males and females

Babies who are at risk of hypoglycaemia, defined as satisfying AT LEAST ONE of the following: 1. Infants of diabetic mothers (any type of diabetes) 2. Preterm (< 37 weeks' gestation) 3. Small (< 2.5kg or < 10th centile on population or customised birthweight chart) 4. Large (> 4.5kg or > 90th centile on population or customised birthweight chart) 5. Other risk e.g. maternal medication

AND satisfy ALL of the following: 1. > or = 35+0 weeks' gestation 2. Birthweight > 2.2kg 3. < 1 hour old 4. No apparent indication for NICU/SCBU admission at time of randomisation 5. Unlikely to require admission to NICU/SCBU for any other reason e.g. respiratory distress 6. Mother intending to breastfeed.

Exclusion Criteria

  1. Major congenital abnormality
  2. Previous formula feed or intravenous fluids
  3. Previous diagnosis of hypoglycaemia
  4. Admitted to NICU/SCBU
  5. Imminent admission to NICU/SCBU

ACTRNACTRN12613000322730

In newborn infants at risk of hypoglycaemia does prophylactic oral dextrose gel compared to placebo reduce the incidence of hypoglycaemia (any blood glucose concentration < 2.6 mM).

Hypoglycaemia Prevention in Newborns with Oral Dextrose: the dosage trial

View record on ANZCTR