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Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of no treatment compared with ibuprofen treatment for patent ductus arteriosus in preterm infants. The study hypothesis is that no treatment is not inferior to oral ibuprofen treatment in preterm infants. (non-inferiority study)


Clinical Trial Description

This study is a randomized, double-blind, placebo-controlled, non-inferiority clinical trial. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02128191
Study type Interventional
Source Samsung Medical Center
Contact
Status Completed
Phase Phase 2
Start date July 2014
Completion date August 2019

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