Study of Interest on Cervical Ultrasound Exploration for Association With Difficult Intubation
NCT ID: NCT02362568
Last Updated: 2016-08-31
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
462 participants
INTERVENTIONAL
2013-10-31
2015-04-30
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
TRIPLE
Study Groups
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Cervical ultrasound exploration
A cervical ultrasound exploration will be performed in all patients admitted for a planned surgery performed under general anesthesia during the stay in the postoperative room.
Ultrasound cervical exploration
The cervical ultrasound exploration will consist in the ultrasound measurement of the length between the hyoid bone and the skin and the length between the thyroid cartilage and the skin. The ultrasound cervical exploration will be performed in all patients admitted in the postoperative room after a planned surgery performed under general anesthesia.
Interventions
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Ultrasound cervical exploration
The cervical ultrasound exploration will consist in the ultrasound measurement of the length between the hyoid bone and the skin and the length between the thyroid cartilage and the skin. The ultrasound cervical exploration will be performed in all patients admitted in the postoperative room after a planned surgery performed under general anesthesia.
Eligibility Criteria
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Inclusion Criteria
* patient consent
Exclusion Criteria
* age under 18
* cervical surgery
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Besancon
OTHER
Responsible Party
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Principal Investigators
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Boinette Romain, MD
Role: PRINCIPAL_INVESTIGATOR
Centre Hospitalier Universitaire de Besancon
Locations
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CHRU de Besançon
Besançon, Franche Comte, France
CHU Besancon Minjoz
Besançon, , France
Countries
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Other Identifiers
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P/2013/181
Identifier Type: -
Identifier Source: org_study_id
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