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
114 participants
OBSERVATIONAL
2021-01-01
2021-10-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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Prone position group
Prone positioning sessions: at least 1 session per day session duration: at least 2 hours
Prone positioning
Prone positioning sessions: at least one session per day proning duration: 2 hours at least per session
Control group
no prone positioning
No interventions assigned to this group
Interventions
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Prone positioning
Prone positioning sessions: at least one session per day proning duration: 2 hours at least per session
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* patients with contraindications of prone positioning: pregnancy, recent abdominal surgery
* patients with pulmonay embolism
* patients requiring invasive mechanical ventilation for extra respiratory reasons: neurological failure, urgent surgery
18 Years
ALL
No
Sponsors
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Mongi Slim Hospital
OTHER
Responsible Party
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Mhamed Sami Mebazaa
Professor head of Anesthesiology and ICU department
Locations
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Mongi Slim hospital
Tunis, , Tunisia
Countries
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Other Identifiers
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COVID PP
Identifier Type: -
Identifier Source: org_study_id
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