Study for Appropriate Operating Table Height for Endotracheal Intubation Under Direct Laryngoscopy
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Purpose
Laryngeal view of the patient and anesthesiologist's discomfort level during endotracheal intubation in relation to the various heights of operating table has not been investigated. The investigators hypothesis is higher table height will improve the laryngeal exposure.
| Condition |
|---|
|
Operating Tables |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Crossover Time Perspective: Prospective |
| Official Title: | Study for Appropriate Operating Table Height for Endotracheal Intubation Under Direct Laryngoscopy |
| Enrollment: | 8 |
| Study Start Date: | March 2010 |
| Study Completion Date: | March 2011 |
| Primary Completion Date: | March 2011 (Final data collection date for primary outcome measure) |
Eight anesthesiologists will be participated. For each anesthesiologist, 20 patients will be enrolled and they will be randomly allocated into one of 4 groups; T10, T8, T6 or T4. The height of operating table will be adjusted prior to commencement of anesthesia induction to place the patient's forehead at one of four anesthesiologist's dermatome levels (T10, T8, T6 or T4) depending on the group. The best laryngeal views will be graded before and after the anesthesiologist's postural change to improve laryngeal visualization of the patient during intubation. Subjective and objective measurement of anesthesiologists' joint flexion during intubation and discomfort ratings for the mask ventilation or intubation will be recorded.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
| Sampling Method: | Non-Probability Sample |
certificated anesthesiologists
Inclusion Criteria:
- have experiences of more than 100 cases of endotracheal intubation
Exclusion Criteria:
- have acute or chronic musculoskeletal disease or pain
Contacts and Locations
More Information
No publications provided
| Responsible Party: | Mi Ja Yun, MD, PhD, Professor, Seoul National University Bundang Hospital |
| ClinicalTrials.gov Identifier: | NCT01649973 History of Changes |
| Other Study ID Numbers: | SeoulNUBH-B-1003-096-012 |
| Study First Received: | July 23, 2012 |
| Last Updated: | July 24, 2012 |
| Health Authority: | Korea: Food and Drug Administration |
ClinicalTrials.gov processed this record on May 19, 2013