McMaster University Medical Centre
Hamilton, Ontario, L8N3Z5, Canada
NCT Number: NCT04494529
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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Notify Me16 year–55 year
Female
Interventional
Phase 3
Hamilton, Ontario, L8N3Z5, Canada
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:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
After the first intramuscular injection of 12 mg of betamethasone, participants randomized to the "Placebo Comparator" group will receive 1 intramuscular injection of placebo.
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.
Time frame: 5-6 months
Feasibility of conducting a full-scale trial will be defined as => 50% recruitment of approached participants
Time frame: 5-6 months
Feasibility of the study intervention will be defined as => 98% compliance with the protocol
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
Time frame: 5-6 months
Pilot clinical data on neonatal mortality, from medical records
Time frame: 5-6 months
Pilot clinical data on respiratory morbidity, from medical records
Time frame: 5-6 months
Pilot clinical data on severe intraventricular haemorrhage, from medical records
Time frame: 5-6 months
Pilot clinical data on severe bowel problems due to necrotizing enterocolitis, from medical records
Time frame: 5-6 months
Pilot clinical data on duration of mechanical ventilation requiring an endotracheal tube, from medical records
Time frame: 5-6 months
Pilot clinical data on need for supplemental oxygen and duration, from medical records
Time frame: 5-6 months
Pilot clinical data on late respiratory morbidity (i.e. bronchopulmonary dysplasia), from medical records
Time frame: 5-6 months
Pilot clinical data on early neonatal sepsis, from medical records
Time frame: 5-6 months
Pilot clinical data on severe late brain injury (periventricular leukomalacia), from medical records
Time frame: 5-6 months
Pilot clinical data on intrauterine fetal demise, from medical records
Time frame: 5-6 months
Pilot clinical data on duration of ventilatory support not requiring an endotracheal tube, from medical records
Time frame: 5-6 months
Pilot clinical data on hypotension < 48 hours of life requiring treatment with hydrocortisone or inotropic medications, from medical records
Time frame: 5-6 months
Pilot clinical data on length of stay in neonatal intensive care unit, from medical records
Time frame: 5-6 months
Pilot clinical data on anthropometry (<10% of expected weight, length, or head circumference for birth week), from medical records
Time frame: 5-6 months
Pilot clinical data on retinopathy of prematurity needing treatment, from medical records
Time frame: 5-6 months
Pilot clinical data on number of infants with patent ductus arteriosus needing a closure procedure, from medical records
Time frame: 18-30 months
Neurosensory/developmental progress at 24 months corrected gestational age, which will consist principally of 2 validated parent-filled questionnaires:
McMaster University
Other
Single Dose Antenatal Corticosteroids (SNACS) Pilot Randomized Control Trial for Women at Risk of Preterm Birth
Acronym: SNACS Pilot
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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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