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
64 participants
OBSERVATIONAL
2024-01-01
2024-08-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Group H
High Flow Anesthesia Group
Oxygen reserve index
Measuring oxygen reserve index during preoxygenation and under general anesthesia
Group M
Minimal Flow Anesthesia Group
Oxygen reserve index
Measuring oxygen reserve index during preoxygenation and under general anesthesia
Interventions
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Oxygen reserve index
Measuring oxygen reserve index during preoxygenation and under general anesthesia
Eligibility Criteria
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Inclusion Criteria
* 18-75 years old
* underwent general anesthesia
* elective ear, nose and throat surgery, lasting longer than 60 minutes
Exclusion Criteria
* those with finger deformities
* unregulated diabetes mellitus, severe heart, kidney, or liver failure, sensitivities to local anesthetics or opioids, those who were morbidly obese (BMI \>40 kg/m²), and breastfeeding women.
18 Years
75 Years
ALL
No
Sponsors
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Sakarya University
OTHER
Responsible Party
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Burak Kaya
Medical Doctor, Specialist
Locations
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Sakarya University Training and Research Hospital
Sakarya, , Turkey (Türkiye)
Countries
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Other Identifiers
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E16214662-050.01.04-8172-213
Identifier Type: -
Identifier Source: org_study_id
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