Selective Early Medical Treatment of Patent Ductus Arteriosus in Extremely Low Gestational Age Infants: A Pilot RCT
Patent Ductus Arteriosus After Premature BirthBackground: 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.
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Participation Requirements
-
Sex:
ALL -
Eligible Ages:
0 to 72
Participation Criteria
Inclusion Criteria:
* Preterm infants less than 26 completed weeks (i.e., up to and including 25 weeks and 6 days) of gestation
Exclusion Criteria:
* 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
Study Location
British Columbia Women's Hospital
British Columbia Women's HospitalVancouver, British Columbia
Canada
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Michael Castaldo
Centre Hospitalier Universitaire de Quebec
Centre Hospitalier Universitaire de QuebecQuébec City, Quebec
Canada
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Audrey Hébert
Stollery Children's Hospital
Stollery Children's HospitalEdmonton, Alberta
Canada
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Abbas Hyderi
Sunnybrook Health Sciences Centre
Sunnybrook Health Sciences CentreToronto, Ontario
Canada
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IWK Health Center
IWK Health CenterHalifax, Nova Scotia
Canada
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Souvik Mitra
Mount Sinai Hospital
Mount Sinai HospitalToronto, Ontario
Canada
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- Study Sponsored By
- IWK Health Centre
- Participants Required
- More Information
- Study ID:
NCT05011149