Ultrasonographic Comparison of Gastric Volume After Three Modes of Positive Facemask During Induction of Anaesthesia
NCT ID: NCT02906267
Last Updated: 2017-07-17
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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UNKNOWN
NA
123 participants
INTERVENTIONAL
2016-12-31
2017-12-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
SINGLE
Study Groups
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Manual-controlled
Patient in the manual ventilation group will receive facemask ventilation to get a tidal volume of 8-10ml/kg with a respiratory rate of 15/min. The pop-off valve will be set to 20 cm H2O.
Diagnostic ultrasonography of gastric volume
Ultrasonic measurement of gastric insufflation during positive pressure ventilation (secondary endpoint) and final gastric volume after positive pressure ventilation (primary endpoint)
Volume-controlled
mechanical breath will be delivered by a Primus ventilator (Dräger, Lubeck, Germany) at a frequency of 15 breath/min. Tidal volume will be set to 8-10 ml/min.
Diagnostic ultrasonography of gastric volume
Ultrasonic measurement of gastric insufflation during positive pressure ventilation (secondary endpoint) and final gastric volume after positive pressure ventilation (primary endpoint)
Pressure-controlled
mechanical breath will be delivered by a Primus ventilator (Dräger, Lubeck, Germany) at a frequency of 15 breath/min. Pressure will be adjusted to obtain a tidal volume of 8-10 ml/min.
Diagnostic ultrasonography of gastric volume
Ultrasonic measurement of gastric insufflation during positive pressure ventilation (secondary endpoint) and final gastric volume after positive pressure ventilation (primary endpoint)
Interventions
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Diagnostic ultrasonography of gastric volume
Ultrasonic measurement of gastric insufflation during positive pressure ventilation (secondary endpoint) and final gastric volume after positive pressure ventilation (primary endpoint)
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
Yes
Sponsors
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University Hospital, Brest
OTHER
Responsible Party
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LAFERE Pierre
Docteur Pierre Lafère
Principal Investigators
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Pierre LAFERE, MD,PhD
Role: PRINCIPAL_INVESTIGATOR
CHRU de Brest
Locations
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CHRU de Brest
Brest, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Ultrasonic gastric volume
Identifier Type: -
Identifier Source: org_study_id
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