drugset / Trial / NCT02351310

Effectiveness of ACS in Extreme Preemies

NCT02351310

Phase 3 Withdrawn Pediatrix
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a randomized prospective clinical study that will evaluate the effects of antenatal corticosteroid administration (ACS) vs. placebo in singleton pregnancies who are threatening to deliver prematurely between 22 0/7 and 23 6/7 weeks on admission with the goal of improving composite neonatal mortality and morbidity.

Timeline

Start
2015-11
Primary completion
2015-11
Completion
2015-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Betamethasone Other / unclassified 12 mg Intramuscular

Indications

No indication recorded.