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Completed

NCT Number: NCT01536158

Oral Paracetamol Versus Oral Ibuprofen in Management of Patent Ductus Arteriosus in Preterm Infants: A Randomised Controlled Trial

The purpose of this study is to determine whether oral paracetamol or ibuprofen has a better or same efficacy and tolerance in closure of patent ductus arteriosus in preterm infants.

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Key information

About this study

To determine whether oral paracetamol or ibuprofen has a better or same efficacy and tolerance in closure of patent ductus arteriosus in preterm infants.

Eighty preterm infants with patent ductus arteriosus will be enrolled in this prospective-randomized study. Patients will receive oral ibuprofen at an initial dose of 10 mg/kg, followed by 5 mg/kg at 24 and 48 h or oral paracetamol 15 mg/kg per dose every 6 hours.

One of the following echocardiographic criteria of a duct size >1.5 mm, a left atrium-to-aorta ratio >1.5, left-to-right shunting of blood, end diastolic reversal of blood flow in the aorta, or poor cardiac function in addition signs of patent ductus arteriosis determined the need of treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Birth weight below 1250 gram
  • Diagnosed patent ductus arteriosus by Echocardiographic examination

Exclusion criteria

  • Accompanied other congenital cardiac anomalies
  • Urine output of less than 1 ml/kg/h during the preceding 8 h,
  • Serum creatinine level >1.6 mg/dl,
  • Platelet count <60,000/mm3,
  • Liver failure,
  • Hyperbilirubinemia requiring exchange transfusion
  • Severe intracranial bleeding (Grade III - IV)
  • Intestinal abnormality and necrotising enterocolitis

Treatment and study plan

Oral paracetamol

Drug

Patients will receive oral paracetamol 15 mg/kg per dose every 6 hours for 3 days.

Other names: Calpol

oral ibuprofen

Drug

Patients will receive oral ibuprofen at an initial dose of 10 mg/kg, followed by 5 mg/kg at 24 and 48 h.

Other names: Pedifen

Primary outcomes

  1. Efficacy and Safety of Oral Paracetamol Versus Oral Ibuprofen

    Time frame: Until discharge

    To compare the closure rate of patent ductus arteriosus after oral paracetamol or oral ibuprofen treatment

Secondary outcomes

  1. Long term effects of oral paracetamol versus oral ibuprofen treatment in preterm infants

    Time frame: corrected 36 weeks or until discharge

    Long term effects such as ROP, BPD,IVH, duration of respiratory support and hospitalization are going to be evaluated.

Sponsors and collaborators

Lead sponsor

Zekai Tahir Burak Women's Health Research and Education Hospital

Other

Registry information

Official study title

Oral Paracetamol Versus Oral Ibuprofen Treatment

Important dates

Study start
2012
Primary completion
2012
Study completion
2012
First posted
Feb 20, 2012
Registry last updated
Dec 27, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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