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Clinical Trial Summary

The purpose of this study is to determine whether helmet is effective as device for noninvasive positive pressure ventilation in the weaning from mechanical ventilation.


Clinical Trial Description

The clinical efficacy of noninvasive positive pressure ventilation (NPPV) has been demonstrated. Interest has emerged in using NPPV to facilitate earlier removal of an endotracheal tube and decrease complications associated with prolonged intubation. Studies assessing NPPV in weaning are not enough and generally are performed with face masks as device for NPPV. This study assesses the efficacy of helmet as device for NPPV during weaning from mechanical ventilation in an ICU and compares this procedure with invasive mechanical complication (IMV) by analyzing respiratory parameters, clinical course and complications. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01322659
Study type Interventional
Source University of Padova
Contact
Status Completed
Phase N/A
Start date March 2010
Completion date January 2013

See also
  Status Clinical Trial Phase
Completed NCT02823392 - Difficult Bag Mask Ventilation and Difficult Intubation in Children
Enrolling by invitation NCT01814306 - Supreme LMA and Proseal LMA in Prone Anesthetized Patient N/A
Terminated NCT01241513 - Induced Changes in Ventilatory Responsiveness and Altitude Exposure Phase 4