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Clinical Trials/NCT02027181
NCT02027181
Completed
Phase 1

Automation of the Oxygen's Administration in Spontaneous Ventilation (FreeO2) During the Hypoxemic Acute Respiratory Distress

University Hospital, Brest4 sites in 2 countries190 target enrollmentAugust 2011

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Acute Respiratory Distress Syndrome
Sponsor
University Hospital, Brest
Enrollment
190
Locations
4
Primary Endpoint
Percentage of time spent in the target zone of oxygen saturation in the acute phase of treatment
Status
Completed
Last Updated
11 years ago

Overview

Brief Summary

Aim: The purpose of this study is to evaluate the use feasibility of FreeO2 so as to deliver automatically oxygen in the emergency department in a patient population admitted for acute respiratory failure.

Hypothesis: The principal hypothesis is that FreeO2 is possible and well-accepted by nurses and medical personnel and there are advantages to use this system. In comparison with the common oxygen delivery (the rotameter), the hypothesis is that FreeO2 system will make for a better control of the oxygen saturation in function of designed target, reducing the desaturation time and hyperoxia. We think that oxygen weaning will be faster than classical way if it is automated. In addition, FreeO2 could reduce the number of intervention by nurse personnel.

Registry
clinicaltrials.gov
Start Date
August 2011
End Date
October 2014
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Admission to the emergency for respiratory disease (or cardiac - acute pulmonary edema)justifying an oxygen administration to over 3 L / min to maintain a SpO2 ≥ 92%.
  • Inclusion within a time less than two hours after the start of the oxygen at the emergency.
  • Patient consent,or a close.

Exclusion Criteria

  • Necessity of an oxygen flow exceeds 15 L / min to maintain a SpO2 higher than 92%.
  • Criteria of gravity justifying immediately a different technique of ventilatory support:
  • Disturbance of consciousness with a Glasgow Coma Score ≤ 12
  • Serious ventricular rhythm disorders
  • Hemodynamic instability (SBP \<80mmHg or recourse to vasopressors)
  • Cardiac or respiratory arrest
  • pH \< 7.35 and PaCO2 \> 55 mm Hg
  • Necessity of a urgent surgery, or coronary revascularization
  • Age \<18 years
  • Pregnant women, lactating

Outcomes

Primary Outcomes

Percentage of time spent in the target zone of oxygen saturation in the acute phase of treatment

Time Frame: 3 hours or 1 hour after after cessation of oxygenation

The target zone of oxygen saturation is : SpO2 = 92-96% The "acute phase of treatment" is defined by the 3 first hours of treatment by oxygenation and/or until one hour after the end of this last.

Secondary Outcomes

  • Frequency of use of invasive or noninvasive ventilation during hospitalization.(28 days max)
  • nursing workload assessed by the number of manual Oxygen flow adjustments and airway management procedures(3 days max)
  • Maintaining EtCO2 in a selected area(3 hours or 1 hour after after cessation of oxygenation)
  • Oxygen consumption measured at the end of administration(3 hours or 1 hour after after cessation of oxygenation)
  • Time spent in a area of severe desaturation (SpO2 <88%) and a hyperoxia area (SpO2> 98%).(3 hours or 1 hour after after cessation of oxygenation)
  • Duration of administration during hospitalization(28 days max)
  • Number of complications related to the administration of oxygen(28 days max)

Study Sites (4)

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