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Early PARacetamol (EPAR) to promote early closure of the ductus arteriosus in preterm infants

Early PARacetamol (EPAR) to promote early closure of the ductus arteriosus in preterm infants

Status
Terminated
Phases
Phase 2
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12616001517460
Acronym
EPAR study
Enrollment
58
Registered
2016-11-03
Start date
2016-11-12
Completion date
2019-03-23
Last updated
2021-02-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The optimal management of PDA is highly controversial with a lack of consensus regarding the need to treat, timing of intervention, the most appropriate pharmacological agents (including dose, dose intervals, duration, repeat courses, routes of administration) and the role of surgical intervention. Traditionally, the medications we use to treat PDA are non-steroidal anti-inflammatory drugs (NSAIDs), which decrease prostaglandin production by inhibiting cyclooxygenases (COX). The most commonly used medications, indomethacin and ibuprofen, have a success rate of approximately 70% - 85%. Unfortunately these medications are associated a number of unwanted adverse effects due to decreased blood flow to the brain, gastrointestinal tract and kidneys. Exposure to these medications puts vulnerable preterm infants at risk of significant complications such as intestinal perforation and necrotising enterocolitis. The alternative to medications is surgical intervention, which also carries significant risks, particularly for extreme preterm infants. Paracetamol is a medication with an excellent safety profile in infants when used to treat mild to moderate pain and fever. Although the mechanism of action of paracetamol is not completely understood, part of its spectrum of activity resembles that of a COX-2 selective inhibitor. Similar to traditional NSAIDs, this results in decreased prostaglandin production. It is therefore intuitive that this may also be effective in promoting ductal closure without the adverse effects associated with NSAIDs. Early experiences with the use of paracetamol for ductal closure have been encouraging. Paracetamol appears to have similar efficacy to NSAIDs, without the gastrointestinal complications associated with NSAIDs, and is well tolerated in the preterm infant population. It has been suggested as a safe alternative medication in situations where other medications have failed or are contraindicated. The aims of this study are to study the effect of early treatment of patent ductus arteriosus with paracetamol and to examine the safety and efficacy profile of paracetamol during the early postnatal period. We hypothesise that early treatment with paracetamol will reduce the number of infants requiring intervention for PDA and that the use of paracetamol in preterm infants with a patent ductus arteriosus will result in a higher rate of ductal closure compared with placebo. We also am to show that paracetamol can be used safely in preterm infants during the early postnatal period.

Interventions

Intravenous paracetamol at a dose of 15 mg/kg (1.5 ml/kg) as a single bolus, followed by 7.5 mg/kg (0.75 ml/kg) every 6 hours for five days

Sponsors

Timothy Schindler
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
No minimum to 6 Hours
Healthy volunteers
No

Inclusion criteria

Preterm infants <6 hours old Born at <29 weeks gestation Informed parental consent Ductus arteriosus characteristics - Patent >1 mm - <30% right to left shunt

Exclusion criteria

Known congenital anomalies Haemodynamic instability (>1 ionotropic agent) Abnormal baseline liver function - Transaminases >50% above upper reference range - Bilirubin above local guideline for exchange transfusion Ductus arteriosus characteristics - <1 mm - >30% right to left shunt

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 20, 2026