Effect of Ketamine+Propofol vs Remifentanyl+Propofol on Laryngeal Mask Insertion Conditions
NCT ID: NCT02583217
Last Updated: 2017-05-08
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
50 participants
OBSERVATIONAL
2015-04-30
2016-01-31
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
PROSPECTIVE
Study Groups
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Ketamine
Ketamine+propofol
Ketamine
To compare ketamine+propofol versus remifentanyl+propofol to maintain good laryngeal mask insertion conditions
propofol
laryngeal mask
Remifentanyl
Remifentanyl+propofol
remifentanyl
propofol
laryngeal mask
Interventions
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Ketamine
To compare ketamine+propofol versus remifentanyl+propofol to maintain good laryngeal mask insertion conditions
remifentanyl
propofol
laryngeal mask
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
FEMALE
No
Sponsors
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Ankara University
OTHER
Responsible Party
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CIGDEM YILDIRIM GUCLU
MD
Principal Investigators
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CIGDEM YILDIRIM GUCLU, MD
Role: PRINCIPAL_INVESTIGATOR
Ankara University
Locations
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Cigdem Yildirim Guclu
Ankara, , Turkey (Türkiye)
Countries
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Other Identifiers
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ANK-42476
Identifier Type: -
Identifier Source: org_study_id
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