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Clinical Trials/NCT01782430
NCT01782430
Unknown
Phase 2

PREoxygenation for the Intubation of Hypoxemic Patients: Comparison of Standard Oxygenation, High Flow Nasal Oxygen Therapy, and NonInvasive Ventilation

University Hospital, Clermont-Ferrand1 site in 1 country132 target enrollmentApril 2015

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Adult Patients
Sponsor
University Hospital, Clermont-Ferrand
Enrollment
132
Locations
1
Primary Endpoint
least pulse oxymetry value
Last Updated
9 years ago

Overview

Brief Summary

Prospective, randomized clinical multicentric study, in ICU, during preoxygenation for the intubation of hypoxemic patients.

Detailed Description

Prospective randomized clinical multicentric study in ICU, comparing standard oxygenation, high flow nasal oxygen therapy and non invasive ventilation (NIV) , with pulse oxymetry values (SpO2), during preoxygenation for hypoxemic patients

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
September 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Clermont-Ferrand
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • adults patients
  • requiring intubation and hypoxemia (defined by PaO2/FiO2 below 200)
  • patient covered by french health care system

Exclusion Criteria

  • patient refusal
  • intubation for other causes (excluding hypoxemia)
  • impossibility to measure pulse oxymetry value
  • contraindication for NIV : vomiting
  • NIV intolerance
  • cardiac arrest during intubation

Outcomes

Primary Outcomes

least pulse oxymetry value

Time Frame: at day 1

Secondary Outcomes

  • Partial pressure of arterial oxygen (PaO2)(at day 1)
  • oxyhemoglobin desaturation below 80 %(at day 1)
  • pulse oxymetry value (at the end of preoxygenation)(at 5 minutes and at 30 minutes after intubation)
  • Regurgitation rate(at day 1)

Study Sites (1)

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