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
97 participants
OBSERVATIONAL
2013-01-01
2013-07-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Group P (n=40) (Propofol),
butanol threshold test and smell identification tests
no additional intervention
Group PS (n=40) (Propofol-Sevoflurane),
butanol threshold test and smell identification tests
no additional intervention
Group S (n=40) (Sevoflurane).
butanol threshold test and smell identification tests
no additional intervention
Interventions
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butanol threshold test and smell identification tests
no additional intervention
Eligibility Criteria
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Inclusion Criteria
* operated under elective conditions with general anesthesia requiring intubation
* operation durations of 40-180 minutes.
Exclusion Criteria
* endocrine or nasal surgery,
* pregnant cases,
* those with history of respiratory tract diseases and psychiatric disease, with disorder of odor reception and perception,
* with smoking and chronic alcohol use,
* requiring a nasogastric probe
18 Years
60 Years
ALL
Yes
Sponsors
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Zonguldak Bulent Ecevit University
OTHER
Responsible Party
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Gamze Küçükosman
medical doctor
Locations
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Gamze Küçükosman
Zonguldak, , Turkey (Türkiye)
Countries
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Other Identifiers
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2013/02
Identifier Type: -
Identifier Source: org_study_id
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