About this trial
Last updated 2 years ago
Study ID
1025627
Status
Recruiting
Type
Observational [Patient Registry]
Placebo
No
Accepting
Up to 12 Years
All
Not accepting
Healthy Volunteers
Trial Timing
Ended 2 years ago
What is this trial about?
Patent ductus arteriosus (PDA) is the most common cardiovascular problem that develops in
preterm infants. Persistent PDA may result in higher rates of death, chronic lung disease
(CLD), pulmonary hemorrhage, necrotizing enterocolitis (NEC), acute kidney injury (AKI),
intraventricular hemorrhage (IVH) and cerebral palsy. Currently available options to treat a
PDA include indomethacin, ibuprofen or acetaminophen followed by surgical or interventional
closure of the PDA if medical therapy fails.
Wide variation exists in PDA treatment practices across Canada. A survey conducted through
the Canadian Neonatal Network (CNN) in 2019 showed that the most common choice of initial
pharmacotherapy is standard dose ibuprofen. In view of the high pharmacotherapy failure rate
with standard dose ibuprofen, there is a growing use of higher doses of ibuprofen with
increasing postnatal age (with 32% of respondents currently adopting this practice) in spite
of the fact that effectiveness and safety of higher ibuprofen doses have not been established
in extremely preterm infants [<29 weeks gestational age (GA)]. In view of this large practice
variation across Canadian neonatal intensive care units (NICUs), we are planning a
comparative effectiveness study of the different primary pharmacotherapeutic agents used to
treat the PDA in preterm infants.
Aims Primary: To compare the primary pharmacotherapeutic practices for PDA closure and
evaluate their impact on clinical outcomes in extremely preterm infants (<29 weeks GA)
Secondary: To understand the relevance of pharmacotherapeutic PDA treatment with respect to
clinical outcomes in the real world.
Methods:
Participants: Extremely preterm infants (<29 weeks gestational age) with an echocardiography
confirmed PDA who will be treated according to attending team
Interventions:
1. Standard dose ibuprofen [10-5-5 regimen, i.e., 10mg/kg followed by 2 doses of 5mg/kg at
24h intervals]
2. Adjustable dose ibuprofen [10-5-5 regimen if treated within the first week. Higher doses
of ibuprofen up to a 20-10-10 regimen if treated after the postnatal age cut-off for
lower dose as per the local center policy]
3. Intravenous indomethacin [0.1-0.3mg/kg every 12-24h for a total of 3 doses].
4. Acetaminophen [Oral/intravenous] (15mg/kg every 6h) for 3-7 days
Outcomes:
Primary: Failure of primary pharmacotherapy (Need for further medical and/or
surgical/interventional treatment following an initial course of pharmacotherapy).
Secondary: (a) Receipt of 2nd course of pharmacotherapy; (b) Surgical/interventional PDA
closure; (c) CLD (d) NEC (stage 2 or greater) (e) Severe IVH (Grade III-IV) (f) Definite
sepsis (g) Stage 1 or greater AKI; (h) Post-treatment serum bilirubin; (i) Phototherapy
duration; (j) All-cause mortality during hospital stay.
What are the participation requirements?
Inclusion Criteria
- Extremely preterm infants (<29 weeks gestational age) with an echocardiography confirmed PDA who will be treated according to attending team
Exclusion Criteria
- Any infant who received pharmacotherapy for a clinically symptomatic PDA without prior echocardiographic confirmation of the presence of PDA will be excluded from all analyses.