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
44 participants
INTERVENTIONAL
2009-05-31
2012-12-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
SINGLE
Study Groups
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Control group
Neutral pressure breathing after 2 min preoxygenation
No interventions assigned to this group
Active group
CPAP 5cm H2O + PSV 5cm H2O breathing after 2 min preoxygenation
CPAP 5 cm H2O + PSV 5 cm H2O
Patients in the intervention group received Continuous Positive Airway Pressure (5 cm H2O) and Pressure Supported Ventilation (5 cm H2O)
Interventions
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CPAP 5 cm H2O + PSV 5 cm H2O
Patients in the intervention group received Continuous Positive Airway Pressure (5 cm H2O) and Pressure Supported Ventilation (5 cm H2O)
Eligibility Criteria
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Inclusion Criteria
* scheduled to undergo elective gastric bypass surgery
* age ≥ 18 years
* ASA Physical Status Classification II-III
Exclusion Criteria
* previous abdominal or thoracic surgery
* inability to comprehend the protocol.
18 Years
60 Years
ALL
Yes
Sponsors
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Karolinska Institutet
OTHER
Responsible Party
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Erik Näslund
Professor
Locations
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Department of Anesthesiology and Intensive Care Danderyd Hospital
Stockholm, , Sweden
Countries
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Other Identifiers
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KIDS CPAP
Identifier Type: -
Identifier Source: org_study_id