Clinical Trials Logo

Clinical Trial 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.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05011149
Study type Interventional
Source IWK Health Centre
Contact Souvik Mitra, MD, MSc
Phone +1-902-470-6490
Email souvik.mitra@iwk.nshealth.ca
Status Recruiting
Phase Phase 3
Start date January 10, 2022
Completion date August 31, 2024

See also
  Status Clinical Trial Phase
Completed NCT04126512 - Timing of Surgical PDA Ligation and Neonatal Outcomes
Recruiting NCT04359134 - Combined Lung Ultrasounds and Transthoracic Electrical Bioimpedance in Preterm Infants With Respiratory Distress.
Recruiting NCT05325177 - PDA Treatment With Ibuprofen and Changes in Tissue Oxygenation. Phase 4
Active, not recruiting NCT03675425 - The Effects of Phototherapy in Preterm Infants Pda N/A
Recruiting NCT04037514 - Paracetamol Versus Ibuprofen in Premature Infants With Hemodynamically Significant Patent Ductus Arteriosus Phase 3
Recruiting NCT05686343 - Hemodynamically Important Patent Ductus Arteriosus in Newborns Under 32 Weeks
Withdrawn NCT04025177 - Indomethacin PK-PD in Extremely Preterm Neonates Phase 2
Recruiting NCT03456336 - Management of the PDA Trial Phase 3
Recruiting NCT05340582 - Co-administration of Acetaminophen With Ibuprofen to Improve Duct-Related Outcomes in Extremely Premature Infants Phase 2
Completed NCT05493540 - Oral Ibuprofen Versus Placebo in Treatment of Patent Ductus Arteriosus (PDA)in Preterm Infants Phase 2