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Weaning Using Noninvasive Positive Pressure Ventilation by Means of Helmet in Patients With Acute Respiratory Failure

NCT01322659 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 250

Last updated 2013-01-31

No results posted yet for this study

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.

Conditions

  • Inadequate or Impaired Breathing Pattern or Ventilation

Interventions

DEVICE

Helmet

Weaning from mechanical ventilation with noninvasive positive pressure ventilation delivered by means of the helmet

DEVICE

Endotracheal tube

Weaning from mechanical ventilation with invasive mechanical ventilation delivered by means of the endotracheal tube

Sponsors & Collaborators

  • University of Padova

    lead OTHER

Principal Investigators

  • Michele Carron, MD · University medical hospital of Padova

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-03-31
Primary Completion
2013-01-31
Completion
2013-01-31

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01322659 on ClinicalTrials.gov