Selective Early Medical Treatment of Patent Ductus Arteriosus in Extremely Low Gestational Age Infants: A Pilot RCT

Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
AgeUp to 72
SponsorIWK Health Centre

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

Qualifiers

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

Treatments tested in this trial

  • Ibuprofen

Treatment groups

100 Participants
are divided into 2 treatment groups

Sponsors and collaborators

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