About this trial
Background: Among preterm infants, those born at a gestational age less than 26 weeks are considered the most vulnerable with a high risk of short- and long-term health problems that include chronic lung disease, brain bleeds, gut injury, kidney failure and death. Patent ductus arteriosus (PDA) is the most common heart condition with almost 70% preterm infants in this gestational age group being diagnosed with a PDA. Though many PDAs spontaneously resolve on their own, research suggests that if the PDA persists, it may contribute to a number of these short- and long-term health problems. Non-steroidal anti-inflammatory medications such as ibuprofen are commonly used to treat a PDA. Such drugs can also have harmful effects on the gut and kidneys of extremely preterm infants. Therefore, we are unsure if early treatment of a symptomatic PDA in this age group is at all beneficial. Given the wide variation in PDA treatment approaches in this age group, a randomized trial design, where extremely preterm infants with a symptomatic PDA are randomly assigned to early treatment or no early treatment, is essential to address this question.
Purpose of the study: The overall purpose of this pilot study is to assess the feasibility of conducting a large study to explore the following research question: In preterm infants born \<26 weeks' gestation, is a strategy of selective early medical treatment of a symptomatic PDA better than no treatment at all in the first week of life?
The main feasibility objectives of this study are:
1. To assess how many eligible infants can be enrolled in the study 2. To assess how many enrolled infants properly complete the study protocol
Importance: To our knowledge this will be the first study on PDA management in preterm infants that specifically aims to enroll preterm infants born at \<26 weeks of gestational age who are at the highest risk for PDA-related problems but have been mostly under-represented in previous PDA studies.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Preterm infants less than 26 completed weeks (i.e., up to and including 25 weeks and 6 days) of gestation
Disqualifiers
no PDA on initial screening echocardiography
congenital heart disease (excluding patent foramen ovale, atrial septal defect or ventricular septal defect with a defect size less than 2mm)
other major congenital anomaly
decision to withhold/withdraw care
Trial design
Parallel
Treatments tested in this trial
Ibuprofen
DrugPharmacotherapy, when indicated (ie, for "severe PDA" on echocardiography, irrespective of clinical symptoms, or a "moderate PDA" on echocardiography with at least moderate clinical illness), will be provided in the form of ibuprofen as first line agent at a standard dosing of 10 mg/kg followed by 2 doses of 5mg/kg every 24 h. The route of administration may be intravenous or enteral, as determined by the treating team. For treated infants, follow-up echocardiography will be conducted at the end of the 3-day course and second course of treatment will be initiated if they still fulfill study treatment criteria as mentioned above. If any treatment-eligible infant has a contraindication to ibuprofen, use of acetaminophen will be permitted as an alternative agent.
Treatment groups
Trial outcomes
Primary outcomes
Proportion of eligible infants recruited during the study period
Proportion of randomized infants with no reported protocol deviations
Secondary outcomes
Proportion of infants in control group meeting pre-defined safety criteria
Reasons for non-recruitment
qualitative description of reasons for non-recruitment of eligible infants
Reasons for non-adherence to protocol
qualitative description of reasons for non-adherence to protocol in randomized infants
Completeness of data collection for clinical outcomes
Proportion of recruited infants with complete clinical outcome data
Sponsors and contacts
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IWK Health Centre
Lead sponsor
BC Children's Hospital Research Institute
Collaborator
CHU de Quebec-Universite Laval
Collaborator
Sunnybrook Health Sciences Centre
Collaborator
Mount Sinai Hospital, Canada
Collaborator
Sharp Mary Birch Hospital for Women & Newborns
Collaborator
Canadian Institutes of Health Research (CIHR)
Collaborator
Dalhousie Medical Research Foundation
Collaborator
Children's Hospital of Orange County
Collaborator
University of Alberta
Collaborator
University of Oklahoma
Collaborator