Preterm Delivery Clinical Trial
Official title:
A Randomized Double-Blinded Study Comparing the Impact of One Versus Two Courses of Antenatal Steroids on Neonatal Outcome
The hypothesis is that administration of two courses of antenatal corticosteroids, compared to one course, will show a 40% reduction in the incidence of composite neonatal morbidity in patients delivering prior to 34 weeks' gestation.
This is a randomized double-blinded placebo-controlled trial. The objective of this study is
to evaluate the impact of one versus two courses of antenatal steroids on the incidence of
major neonatal morbidity including respiratory distress syndrome in patients delivering
prior to 34 weeks' gestation in a randomized prospective fashion.
Preterm delivery occurs in approximately 10% of all deliveries in the United States. Preterm
birth is the cause of 75% of neonatal mortality not mentioning the significantly increased
morbidity from respiratory distress syndrome, intraventricular hemorrhage, necrotizing
enterocolitis, and sepsis. Numerous studies have evaluated the safety and efficacy of
antenatal corticosteroid (ACS) administration in threatened preterm labor.
National Institutes of Health (NIH) first consensus conference in 1994 evaluated the
research in this field. Conclusions included the clear evidence that antenatal
corticosteroids decrease the incidence of RDS in infants born at 29-34 weeks gestation, with
a decrease in RDS severity for infants born at 24-28 weeks gestation and a decrease in the
incidence of intraventricular hemorrhage in infants born at 24-28 weeks gestation without
harm to mother or fetus. Their recommendation was to give a single course of corticosteroids
to all pregnant women between 24 and 34 weeks gestation who are at risk of preterm delivery
within 7 days.
Since the studies on the duration of the effects of antenatal corticosteroids in the fetus
are not conclusive, many obstetricians repeat corticosteroids weekly or bi-weekly to
patients continuing to be at risk for preterm delivery. Lacking scientific evidence, many
investigators have performed retrospective analyses regarding the effects of single-course
versus multiple-course antenatal corticosteroids.
The NIH consensus panel reconvened in 2000 and concluded that studies regarding repeated
courses of corticosteroids are suggestive of possible benefits, especially in reduction of
RDS, however, design flaws limit their validity.
The more recent publication from Caughey and Parer examined the literature for evidence
regarding a dose response of the benefits and detriments of antenatal corticosteroids. Based
on their complex mathematical analysis they recommend all fetus' between 24 and 34 weeks'
gestation at risk for preterm delivery should be given a first course of ANC. If the risk of
preterm delivery persists the next course should be given 2 weeks later, for a maximum of
two courses. Consistent with all previous articles, the call for a well designed randomized,
controlled trial is made.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention
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