CompletedPhase 2Phase 3ACTRN12612000584831

STRIDER (NZAus): A randomised placebo-controlled trial of a new therapy (sildenafil) to help growth in severely growth restricted fetuses at very early gestations.

STRIDER (NZAus): A randomised placebo controlled trial of sildenafil therapy to improve fetal growth velocity in dismal prognosis early-onset intrauterine growth restriction (New Zealand and Australia).


Sponsor

University of Auckland

Enrollment

122 participants

Start Date

Mar 11, 2014

Study Type

Interventional

Conditions

Summary

Intrauterine growth restriction (IUGR) describes conditions where fetuses are smaller than expected for their gestational age. This puts the fetus at risk of death, hypoxia and preterm birth. If IUGR occurs early in pregnancy (i.e before 28 weeks gestation) survival rates are only 70% and survival free of major handicap (intact survival) is much lower at 20%. Current management involves intensive fetal surveillance and delivery when there is evidence of serious compromise (to avoid death in utero) but this leads to the consequent risks of prematurity. There is no known treatment for IUGR. This is a double blind randomised placebo controlled trial of Sildenafil, a nitric oxide donor drug, that has the potential to vasodilate uteroplacental vessels improving placental function. It may represent a novel therapy for IUGR. It has been used in pregnancy without adverse events and in a small case-control study it improved daily fetal growth velocity. Women with severe early onset IUGR will be invited to take part in the study at MFM units across NZ and Australia. This study will demonstrate if Sildenafil improves fetal growth, the results will be used in collaboration with other similar studies planned worldwide to demonstrate if Sildenafil improves rates of survival free of major handicap. This trial incorporates the STRIDER NZAus Childhood Outcome Study: a follow up assessment of all surviving children at 2-3 years’ corrected age to determine whether any benefit (or harm) seen in the newborn as a consequence of antenatal sildenafil therapy is sustained, or develops, through childhood.


Eligibility

Sex: Females

Inclusion Criteria3

  • Singleton pregnancy.
  • a. At 22+0 weeks to 27+6 weeks: AC measure less than or equal to 3 percentile for gestational age; OR
  • b. At 28+0 weeks to 29+6 weeks ultrasound estimate of fetal weight (EFW) <700grams.

Exclusion Criteria5

  • Known major fetal anomaly/syndrome/congenital infection deemed to be the likely cause of IUGR.
  • Known fetal aneuploidy.
  • Already made plan for termination of pregnancy.
  • Maternal disease (e.g. pre-eclampsia) where it is expected that delivery is necessary within 48 hours.
  • Any contraindication to sildenafil therapy.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

Sildenafil 25mg three times a day as an oral tablet from randomisation until delivery (or 32 weeks gestation, whichever occurs first).

Sildenafil 25mg three times a day as an oral tablet from randomisation until delivery (or 32 weeks gestation, whichever occurs first).


Locations(1)

New Zealand

View Full Details on ANZCTR

For the most up-to-date information, visit the official listing.

Visit

ACTRN12612000584831