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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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8 January 2024 |
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Main ID: |
NCT02482870 |
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Date of registration:
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22/06/2015 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Efficiency of the King Vision Video Laryngoscope
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Scientific title:
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Comparison of King Vision Video Laryngoscope and Macintosh Laryngoscope in Terms of First Pass Intubation Success Rate, Intubation Time, Glottic View Time, and Complications Related to Laryngoscopy |
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Date of first enrolment:
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January 2014 |
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Target sample size:
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388 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/ct2/show/NCT02482870 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Sequential Assignment. Primary purpose: Other. Masking: Double (Participant, Outcomes Assessor).
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Phase:
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N/A
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Countries of recruitment
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Turkey
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Contacts
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Name:
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Basar Erdivanli, Asst. Prof. |
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Address:
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Telephone:
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Email:
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Affiliation:
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Recep Tayyip Erdogan Univeristy, Medical Faculty, Department of Anesthesiology and Reanimation |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- scheduled for general anesthesia
- age higher than 18 years
- age lower than 60 years
Exclusion Criteria:
- emergency surgery
- mouth opening less than 2 cm
- American Society of Anesthesiologists (ASA) score higher than 2
- oropharyngeal anomaly
- glottic or supraglottic mass
- history of surgery due to oropharyngeal anomaly, glottic or supraglottic mass
Age minimum:
18 Years
Age maximum:
60 Years
Gender:
All
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Health Condition(s) or Problem(s) studied
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Intubation
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Respiratory Failure
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Intervention(s)
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Device: Macintosh laryngoscope
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Device: King Vision video laryngoscope
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Primary Outcome(s)
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Intubation Success Rate
[Time Frame: less than 24 hours]
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Secondary Outcome(s)
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Airway Complications
[Time Frame: The participants' will be followed for the duration of hospital stay, an expected average of 2 days]
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Glottic View Time
[Time Frame: less than 24 hours]
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Intubation Time
[Time Frame: less than 24 hours]
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Cormack-Lehane Score
[Time Frame: less than 24 hours]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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