Status:

TERMINATED

Evaluation of Oxygen Therapy Delivery Systems in Hypoxemic Acute Respiratory Failure

Lead Sponsor:

Nantes University Hospital

Conditions:

Acute Respiratory Failure

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The main objective of this study is to evaluate the efficiency of the oxygen therapy delivery system Optiflow® compared to 2 others standard oxygen therapy delivery systems (Ospal®, non invasive venti...

Eligibility Criteria

Inclusion

  • Patient hospitalized in the intensive care unit of Nantes University Hospital
  • Signed informed consent
  • Patient with not hypercapnic acute hypoxemic respiratory failure
  • Immunocompetent and immunodeficient patient

Exclusion

  • Age \< 18 years
  • Pregnancy
  • Contra-indication to non invasive ventilation
  • Allergy to xylocaine
  • Coagulation troubles
  • Tracheotomized patient
  • Urgent indication to intubation
  • Hypercapnic acute respiratory failure
  • Acute pulmonary edema
  • Face or nose malformation

Key Trial Info

Start Date :

November 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2013

Estimated Enrollment :

16 Patients enrolled

Trial Details

Trial ID

NCT01243918

Start Date

November 1 2010

End Date

June 1 2013

Last Update

October 7 2013

Active Locations (1)

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1

Nantes University Hospital

Nantes, France