Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
20 participants
INTERVENTIONAL
2011-02-28
2013-06-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
SUPPORTIVE_CARE
NONE
Study Groups
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High Flow Oxygen
Patients receiving oxygen via high flow oxygen therapy (Optiflow)
Optiflow
patients receive oxygen via high flow oxygen therapy during 20 minutes
Conventionnal
patients receiving oxygen via conventional way (low flow)
No interventions assigned to this group
Interventions
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Optiflow
patients receive oxygen via high flow oxygen therapy during 20 minutes
Eligibility Criteria
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Inclusion Criteria
* Patient under mechanical ventilation, during respiratory weaning.
Exclusion Criteria
* Neuromuscular disease, altered consciousness or agitation for patients under mechanical ventilation.
18 Years
90 Years
ALL
No
Sponsors
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Cliniques universitaires Saint-Luc- Université Catholique de Louvain
OTHER
Responsible Party
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Bialais
physiotherapist PhD student
Principal Investigators
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Emilie Bialais, PhD Student
Role: PRINCIPAL_INVESTIGATOR
Cliniques universitaires Saint-Luc- Université Catholique de Louvain
Other Identifiers
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OptSCM
Identifier Type: -
Identifier Source: org_study_id
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