Co-administration of Acetaminophen With Ibuprofen to Improve Duct-Related Outcomes in Extremely Premature Infants

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
AgeUp to 27
SponsorMount Sinai Hospital, Canada

About this trial

Patent ductus arteriosus (PDA), the most common cardiovascular complication of prematurity, is associated with higher mortality and morbidities in extremely low gestational age neonates (ELGANs, \< 27+0 weeks). Ibuprofen and acetaminophen, which act by reducing prostaglandin synthesis, are the most commonly used first and second line agents for PDA treatment across Canada. However, initial treatment failure with monotherapy is a major problem, occurring in \>60% ELGANs. Treatment failure is associated with worsening rates of mortality and bronchopulmonary dysplasia (BPD), while early treatment success can achieve rates comparable to neonates without PDA. Treatment failure resulting in prolonged disease exposure is thought to be a major contributor. Recently, combination therapy with acetaminophen and ibuprofen has emerged as a new treatment regime. Acetaminophen exerts anti-prostaglandin effect through a different receptor site than ibuprofen, providing a biological rationale for their synergistic action.

The objective of this study is to evaluate the clinical impact, efficacy and safety of combination regime (Ibuprofen + IV Acetaminophen) for the first treatment course for PDA in ELGANs vs. Ibuprofen alone (current standard treatment).

The study will also evaluate the effects of combination regime vs. ibuprofen alone on neurodevelopmental outcomes at 18-30 months corrected age.

Eligibility criteria

Qualifiers

Preterm infants born <27+0 weeks gestational age

Permission given by the attending clinician to approach and then consent obtained from parents

Diagnosis of PDA ≥ 1.5 mm on echocardiography with unrestrictive predominantly left to right shunt

Designated to receive first treatment course with intravenous or enteral ibuprofen, as decided by the attending team.

Disqualifiers

Chromosomal anomaly

Pre-treatment renal dysfunction defined as urine output < 1ml/kg/hour for the previous 24 hours or serum creatinine > 100 micromol/L

Pre-treatment hepatic dysfunction defined as serum aminotransferase (ALT) > 100 units/L94

Platelet count <50,000 per microliter

Trial design

Treatments tested in this trial

  • Acetaminophen Injection
  • Ibuprofen 20 mg/mL oral suspension or Ibuprofen lysine 10 mg/mL injection solution (Neoprofen)
  • Sodium chloride 0.9% injection

Treatment groups

310 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Mount Sinai Hospital, Canada

Lead sponsor

Sunnybrook Health Sciences Centre

Collaborator

McMaster Children's Hospital

Collaborator

The Rotunda Hospital

Collaborator

John Hunter Hospital

Collaborator

Royal Alexandra Hospital

Collaborator

Centre de Recheche du Centre Hospitalier Université Laval

Collaborator

Royal North Shore Hospital

Collaborator

Prince of Wales Hospital, Shatin, Hong Kong

Collaborator