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Completed

NCT Number: NCT04494529

Single Dose Antenatal Corticosteroids (SNACS) for Women at Risk of Preterm Birth

Antenatal corticosteroids (ACS) reduce the risks of neonatal death and morbidities, such as respiratory distress syndrome, in preterm infants.

Standard of care for women at risk of preterm birth includes 2 doses of 12 mg betamethasone (for a total of 24 mg) to accelerate fetal lung maturity.

We plan to conduct a pilot clinical trial to determine the feasibility of a trial comparing half the usual dose (total 12 mg) of betamethasone to the standard double dose (total 24 mg) of betamethasone.

The results of this pilot will be combined with the full-scale RCT (NCT05114096) for which we have received funding from the Canadian Institutes of Health Research (CIHR).

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Key information

Age range

16 year–55 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

McMaster University Medical Centre

Hamilton, Ontario, L8N3Z5, Canada

About this study

Preterm infants are at risk of mortality and morbidity. Antenatal corticosteroids (ACS) reduce the risks of neonatal death and morbidities, such as respiratory distress syndrome.

Standard of care for women at risk of preterm birth includes 2 doses of 12 mg betamethasone (for a total of 24 mg) to accelerate fetal lung maturity. There are no published clinical trial data on the benefits or risks of a single dose of antenatal corticosteroid vs. standard double doses.

Pilot trials are now viewed as an "almost essential prerequisite" to large, expensive, full scale studies. Thus, we plan to conduct a pilot clinical trial to determine the feasibility of a trial comparing half the usual dose (12 mg of betamethasone + placebo) to the standard double dose (12 mg + 12 mg of betamethasone), as well as the feasibility of the study protocol. Secondary outcomes will include process outcomes and pilot clinical outcomes, that will be combined with the full-scale RCT for which we have received funding from CIHR.

We plan to conduct a 24-month corrected gestational age follow-up, which will consist principally of 2 validated parent-filled questionnaires:

  • Ages and Stages Questionnaire-3 (ASQ)
  • Child Behavior Checklist
  • A single question parent report of whether there has been a physician diagnosis of cerebral palsy. (recommended by our parent partners)

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Pregnant women at risk of preterm birth with a singleton or twins between =>22+0/7 and <=34+6/7 weeks' gestation
  • Pregnant with either singletons or twins
  • Has already received the first dose of 12 mg intramuscular betamethasone within the past 24 hours
  • All fetuses are alive and without compromise as per ultrasound or fetal heart monitor
  • Is capable of giving informed, written consent in English

Exclusion criteria

  • Any contraindications to receiving corticosteroids
  • Requires chronic doses of corticosteroids secondary to a medical condition (e.g. systemic lupus erythematosus, severe asthma, congenital adrenal hyperplasia, etc.)
  • Received any prior doses of antenatal corticosteroids except for the 1st dose of 12 mg intramuscular betamethasone
  • Had any previous participation in this trial
  • Pregnant with a fetus with severe congenital anomaly (e.g. anencephaly, transposition of the great arteries, etc.) or major chromosomal abnormalities (e.g. Trisomy 18, Trisomy 21, etc.)
  • Pregnant with monoamniotic/monochorionic (Mono/Mono) twins

Treatment and study plan

12 mg betamethasone + placebo

Drug

After the first intramuscular injection of 12 mg of betamethasone, participants randomized to the "Placebo Comparator" group will receive 1 intramuscular injection of placebo.

24 mg betamethasone

Drug

After the first intramuscular injection of 12 mg of betamethasone, participants randomized to the "Active Comparator" group will receive the standard 2nd intramuscular injection of 12 mg of betamethasone.

Primary outcomes

  1. Feasibility of conducting a full-scale trial

    Time frame: 5-6 months

    Feasibility of conducting a full-scale trial will be defined as => 50% recruitment of approached participants

  2. Feasibility of the study protocol

    Time frame: 5-6 months

    Feasibility of the study intervention will be defined as => 98% compliance with the protocol

Secondary outcomes

  1. Process outcomes

    Time frame: 5-6 months

    The proportions of patients who: will be approached by the circle of care, and will agree to be approached by the research team, and will agree to participate

  2. Neonatal mortality rates

    Time frame: 5-6 months

    Pilot clinical data on neonatal mortality, from medical records

  3. Respiratory morbidity rates

    Time frame: 5-6 months

    Pilot clinical data on respiratory morbidity, from medical records

  4. Severe intraventricular haemorrhage rates

    Time frame: 5-6 months

    Pilot clinical data on severe intraventricular haemorrhage, from medical records

  5. Rates of severe bowel problems due to necrotizing enterocolitis

    Time frame: 5-6 months

    Pilot clinical data on severe bowel problems due to necrotizing enterocolitis, from medical records

  6. Duration of mechanical ventilation requiring an endotracheal tube

    Time frame: 5-6 months

    Pilot clinical data on duration of mechanical ventilation requiring an endotracheal tube, from medical records

  7. Need for supplemental oxygen and duration

    Time frame: 5-6 months

    Pilot clinical data on need for supplemental oxygen and duration, from medical records

  8. Late respiratory morbidity (i.e. bronchopulmonary dysplasia) rates

    Time frame: 5-6 months

    Pilot clinical data on late respiratory morbidity (i.e. bronchopulmonary dysplasia), from medical records

  9. Early neonatal sepsis rates

    Time frame: 5-6 months

    Pilot clinical data on early neonatal sepsis, from medical records

  10. Severe late brain injury (periventricular leukomalacia) rates

    Time frame: 5-6 months

    Pilot clinical data on severe late brain injury (periventricular leukomalacia), from medical records

  11. Intrauterine fetal demise rates

    Time frame: 5-6 months

    Pilot clinical data on intrauterine fetal demise, from medical records

  12. Duration of ventilatory support not requiring an endotracheal tube

    Time frame: 5-6 months

    Pilot clinical data on duration of ventilatory support not requiring an endotracheal tube, from medical records

  13. Rates of hypotension < 48 hours of life requiring treatment with hydrocortisone or inotropic medications

    Time frame: 5-6 months

    Pilot clinical data on hypotension < 48 hours of life requiring treatment with hydrocortisone or inotropic medications, from medical records

  14. Length of stay in neonatal intensive care unit

    Time frame: 5-6 months

    Pilot clinical data on length of stay in neonatal intensive care unit, from medical records

  15. Anthropometry composite (<10% of expected weight, length, or head circumference for birth week)

    Time frame: 5-6 months

    Pilot clinical data on anthropometry (<10% of expected weight, length, or head circumference for birth week), from medical records

  16. Number of infants with retinopathy of prematurity needing treatment

    Time frame: 5-6 months

    Pilot clinical data on retinopathy of prematurity needing treatment, from medical records

  17. Patent ductus arteriosus needing a closure procedure

    Time frame: 5-6 months

    Pilot clinical data on number of infants with patent ductus arteriosus needing a closure procedure, from medical records

  18. 24-month follow-up

    Time frame: 18-30 months

    Neurosensory/developmental progress at 24 months corrected gestational age, which will consist principally of 2 validated parent-filled questionnaires:

    • Ages and Stages Questionnaire-3 (ASQ)
    • Child Behavior Checklist
    • A single-question parent report of whether there has been a physician diagnosis of cerebral palsy.

Sponsors and collaborators

Lead sponsor

McMaster University

Other

Registry information

Official study title

Single Dose Antenatal Corticosteroids (SNACS) Pilot Randomized Control Trial for Women at Risk of Preterm Birth

Acronym: SNACS Pilot

Important dates

Study start
2021
Primary completion
2021
Study completion
2021
First posted
Jul 31, 2020
Registry last updated
Aug 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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