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Clinical Trial Summary

This is a prospective, observational, multicenter study conducted during 1 year in adult and paediatric intensive care units equipped with the EZ-KINOX™ system.

A maximum of 250 patients (newborns to adults, suffering from Pulmonary Arterial Hypertension (PAH) associated with cardiac surgery or Persistent Pulmonary Hypertension in the Newborn (PPHN) receiving iNO through the integrated delivery and monitoring EZ-KINOX™ system was planned to be included.

The study is strictly non-interventional with the aim of describing current practices and therefore did not affect the patient usual management.


Clinical Trial Description

This study is intended to describe daily practice and therefore, there is not a standardized protocol but only patient-based and site-based questionnaires. ;


Study Design

Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02821156
Study type Observational
Source Air Liquide Santé International
Contact
Status Completed
Phase N/A
Start date September 2014
Completion date October 2015

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