Overview
Late Preterm Corticosteroids and Neonatal Hypoglycemia
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-07-01
2024-07-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
This is a prospective randomized controlled trial investigating the timing of betamethasone administration in late preterm infants in relation to delivery and impact on neonatal hypoglycemia. Previous data has shown that neonatal hypoglycemia is increased in late preterm infants that were exposed to antenatal corticosteroids. The investigators hypothesize that the timing of steroid administration may impact the development of neonatal hypoglycemia.Phase:
Phase 4Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
University of Southern CaliforniaTreatments:
Betamethasone
Betamethasone benzoate
Betamethasone sodium phosphate
Betamethasone Valerate
Betamethasone-17,21-dipropionate
Criteria
Inclusion Criteria:- Singleton pregnancy
- Gestational age 34 0/7 weeks to 36 5/7 weeks
- Planned delivery in late preterm period
Exclusion Criteria:
- Prior course of betamethasone during pregnancy
- Twin gestation
- Fetal demise
- Major fetal anomaly
- Maternal contraindication to betamethasone
- Pregestational diabetes
- Expected delivery within 12 hours of randomization