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

This trial does not accept healthy volunteers

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

Design model

Parallel

Treatments tested in this trial

  • Ibuprofen

    Drug

    Pharmacotherapy, 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

100 Participants
are divided into 2 treatment groups
Group A: Selective early medical treatment (SMART) strategyExperimental treatment 1 intervention
Group B: Early conservative management strategyNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Proportion of eligible infants recruited during the study period

Time frame
7 days postnatal age
2

Proportion of randomized infants with no reported protocol deviations

Time frame
7 days postnatal age

Secondary outcomes

1

Proportion of infants in control group meeting pre-defined safety criteria

Time frame
7 days postnatal age
2

Reasons for non-recruitment

qualitative description of reasons for non-recruitment of eligible infants

Time frame
7 days postnatal age
3

Reasons for non-adherence to protocol

qualitative description of reasons for non-adherence to protocol in randomized infants

Time frame
7 days postnatal age
4

Completeness of data collection for clinical outcomes

Proportion of recruited infants with complete clinical outcome data

Time frame
through hospital discharge (approximately 20 weeks postnatal age unless death occurs first)

Other outcomes

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