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โ† Trials
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Maternal Oxygen Supplementation for Intrauterine Resuscitation

RecruitingNAAges any - anyFemaleWashington University School of Medicine
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In plain words

What the trial is, and whether it could suit you

More than 80% of the 3 million women who labor and deliver each year in the United States undergo continuous electronic fetal monitoring (EFM) during labor in order to fetal hypoxia and prevent the transition to acidemia, expedited operative delivery, and/or neonatal morbidity. Category II EFM is the most commonly observed group of fetal heart rate features in labor. One common response to Category II EFM is maternal oxygen (O2) supplementation. The theoretic rationale for O2 administration is that it increases O2 transfer to a hypoxic fetus. There are conflicting national guidelines regarding O2 administration - the American College of Obstetricians and Gynecologists suggest O2 is ineffective, whereas the Association of Women's Health, Obstetric, and Neonatal Nurses recommend continued use given lack of definitive data on safety and efficacy. A recent national survey of nearly 600 Labor

Sign in to get the eligibility rules as simple questions to take to your doctor.

๐Ÿ“‹ Eligibility rules (as published)
Inclusion Criteria: * Singleton gestation * Gestational age\>=37 weeks * Spontaneous labor or induction of labor * English or spanish speaking * Planned continuous fetal monitoring Exclusion Criteria: * Preterm gestation * Major fetal anomaly * Multiple gestation * Category III fetal monitoring at time of admission * Maternal hypoxia \<95% * Planned or scheduled cesarean delivery Excluded from randomization if receiving nitrous oxide for analgesia at time of randomization.
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What it tests

  • Maternal oxygen supplementation
  • Room air
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Where

1 site
Barnes Jewish Hospital
St Louis, United States
๐Ÿค Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible โ€” always decide together with your own doctor.
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