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Cross-over Comparison of the V60 System to Other Bi-Level Noninvasive Ventilators

Respiratory Failure Clinical Trial

Official title:
Cross-over Comparison of the V60 System to Other Bi-Level Noninvasive Ventilators for Adult Patients With Respiratory Failure or Respiratory Insufficiency

Clinical Trial Summary

The purpose of this study is to compare a new noninvasive ventilator to existing ventilators already used for patient care.

Clinical Trial Description

The primary objective of this study was to compare the performance (i.e., patient self-reported Comfort score) of the V60 device and a conventional noninvasive ventilator (patient's current ventilator). For the User Needs Assessment, the primary objective of the study was to validate the V60 to user needs. All patients were volunteers from the Respiratory Section of the Health Sciences Centre at the University of Manitoba. The study utilized a randomized 2-period cross-over study design to compare the V60 System to the patients' existing conventional noninvasive ventilator in different ventilation modes. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00817297
Study type Interventional
Source Respironics, California, Inc.
Contact
Status Completed
Phase N/A
Start date January 17, 2009
Completion date April 7, 2009
View Details
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