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Paracetamol And Ibuprofen/Indomethacin in Closing Patent Ductus Arteriosus — PAI  

Patent Ductus Arteriosus Clinical Trial

Official title:
Paracetamol And Ibuprofen/Indomethacin in Closing Patent Ductus Arteriosus of Preterm Infants - Randomised, Placebo-controlled Multicentre Trial

Clinical Trial Summary

The purpose of this pilot trial is to study efficacy and safety of simultaneous intravenous (iv) ibuprofen/indomethacin and paracetamol medications in the closure of patent ductus arteriosus (PDA) in preterm infants. It is randomized, placebo-controlled, double-blind, phase 1, multicenter, clinical trial.

Clinical Trial Description

Premature infants (born before 37 weeks gestational age) with patent ductus arteriosus (PDA) are the focus of the study since no trials on the additive efficacy of these two medications on the contraction of ductus arteriosus are available. Preterm infants who are diagnosed to have a hemodynamically significant PDA and who, according to the decision of the attending clinician, need ibuprofen/indomethacin therapy, are eligible to this trial. If the parents deny the consent, the patient will be treated according to the standard PDA treatment: three days' iv ibuprofen Pedea® 5mg/ml solution infusion (Oulu, Helsinki, Tartu) dosing: 10mg/kg + 5mg/kg + 5mg/kg (q24h); or three days' iv indomethacin (Turku) 0.2mg/kg + 0.1mg/kg + 0.1mg/kg (q24h). In case of any contraindications for ibuprofen/indomethacin, the treatment would be surgical ligation. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03648437
Study type Interventional
Source University of Oulu
Contact Outi Aikio, MD, PhD
Phone +35883155810
Email outi.aikio@pohde.fi
Status Recruiting
Phase Phase 1
Start date September 3, 2018
Completion date March 1, 2024
View Details
See also
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