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

Last updated: June 18, 2024
Sponsor: IWK Health Centre
Overall Status: Active - Recruiting

Phase

3

Condition

N/A

Treatment

Ibuprofen

Clinical Study ID

NCT05011149
459750
  • Ages < 72
  • All Genders

Study Summary

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

Inclusion

Inclusion Criteria:

  • Preterm infants less than 26 completed weeks (i.e., up to and including 25 weeks and 6 days) of gestation

Exclusion

Exclusion Criteria:

  • no PDA on initial screening echocardiography

  • congenital heart disease (excluding patent foramen ovale, atrial septal defect orventricular septal defect with a defect size less than 2mm)

  • other major congenital anomaly

  • decision to withhold/withdraw care

Study Design

Total Participants: 100
Treatment Group(s): 1
Primary Treatment: Ibuprofen
Phase: 3
Study Start date:
January 10, 2022
Estimated Completion Date:
September 30, 2024

Connect with a study center

  • Stollery Children's Hospital

    Edmonton, Alberta
    Canada

    Active - Recruiting

  • British Columbia Women's Hospital

    Vancouver, British Columbia
    Canada

    Active - Recruiting

  • IWK Health Center

    Halifax, Nova Scotia B3K 6R8
    Canada

    Active - Recruiting

  • Mount Sinai Hospital

    Toronto, Ontario
    Canada

    Site Not Available

  • Sunnybrook Health Sciences Centre

    Toronto, Ontario
    Canada

    Site Not Available

  • Centre Hospitalier Universitaire de Quebec

    Québec City, Quebec
    Canada

    Active - Recruiting

  • Children's Hospital of Orange County

    Orange, California 92868
    United States

    Active - Recruiting

  • Sharp Mary Birch Hospital for Women & Newborns

    San Diego, California 92123
    United States

    Terminated

  • OU College of Medicine, University of Oklahoma

    Oklahoma City, Oklahoma 73117
    United States

    Active - Recruiting

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