About this trial
In Canada, about 900 babies each year are born very early (\<26 weeks of gestation) and have a high chance of dying or having a serious bleed in the brain. Families of these extremely preterm babies consider preventing severe brain bleeding as critical to their child's health and well-being. A medicine called indomethacin, when given intravenously in 3-doses, is known to reduce severe brain bleeding. But use of this drug is variable among clinicians working in the neonatal intensive care unit (NICU) due to (a) its side effects on the gut; (b) possible harm when used with other medications; (c) a notion that despite reducing brain bleeds, the child's long-term brain development is not improved. Emerging evidence suggests that a single low-dose indomethacin regimen may be equally effective in reducing severe brain bleeding as compared to a traditional 3-dose regimen.
The investigators propose a blinded randomized controlled trial, a study design where babies born \<26 weeks will be randomly assigned within 12 hours of birth to either a single dose of intravenous indomethacin or similar looking placebo in the form a saline solution. The study will test if a single dose indomethacin regimen is effective in improving survival of these babies without the devastating complication of severe brain bleeding. In this study the care providers and researchers will be unaware as to which baby receives indomethacin and which baby receives placebo to ensure no one's expectations or biases can influence the results.
The investigators will conduct the study in multiple NICUs across Canada, the United States and Australia in 2 phases: First, an internal pilot phase that will enroll 104 babies born \<26 weeks or \<750 g birth weight over a period of 1 year. If the investigators are successful in achieving their target enrolment in the pilot phase, they will move on to the second phase and continue enrollment up to a total of 500 babies born \<26 weeks or \<750 g birth weight over a period of 3 years. The total of 500 babies will include the 104 babies enrolled in the first phase of the study. This study will help the investigators determine in the most unbiased way whether a single dose of indomethacin given immediately after birth in the smallest babies born \<26 weeks of gestation can safely and effectively reduce severe brain bleeding.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Extremely preterm infants born <26 completed weeks of GA and/or extremely low BW infants born <750g
Disqualifiers
antenatal diagnosis of duct dependent CHD
acute hypoxic respiratory failure [defined as fraction of inspired oxygen (FiO2)>0.60 for ≥2h)
inhaled nitric oxide (iNO) therapy due to suspected or confirmed acute pulmonary hypertension (PH)
receipt of prophylactic or therapeutic hydrocortisone
Trial design
Parallel
Treatments tested in this trial
Indomethacin
DrugSingle dose of 0.1 mg/kg dose intravenous indomethacin as a slow infusion over 20 mins
Placebo
DrugSingle dose of intravenous normal saline placebo as a slow infusion over 20 mins
Treatment groups
Trial outcomes
Primary outcomes
Survival without severe intraventricular hemorrhage (sIVH)
Any IVH more than grade 2 (i.e., grade 3, grade 4/intraparenchymal hemorrhage/perventricular hemorrhagic infarction is classified as sIVH
Secondary outcomes
Mortality
Severe IVH
Any IVH more than grade 2 (i.e., grade 3, grade 4/intraparenchymal hemorrhage/perventricular hemorrhagic infarction is classified as sIVH
Gastrointestinal perforation
Necrotizing enterocolitis (NEC)
Bell Stage ≥stage 2
Other outcomes
Pharmacokinetic outcomes
clearance, volume of distribution and plasma exposure of single-dose indomethacin
Health Economic outcomes
Total healthcare costs (measured to first discharge home); cost per sIVH or death averted; and cost per death averted
Primary feasibility outcomes (during the internal pilot)
(1) Proportion of eligible infants randomized during the internal pilot; (2) Proportion of randomized infants with no reported protocol deviation during the internal pilot
Secondary feasibility outcomes (during the internal pilot)
(1) Reasons for non-recruitment and non-adherence to protocol; (2) qualitative views of parents and neonatologists on recruitment strategies
Sponsors and contacts
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