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Clinical Trials/NCT02502422
NCT02502422CompletedNot Applicable

Prediction of Optimal Laryngeal Mask Airway Cuff Volume From Parameters of Physical Examination of Head and Neck

Korea University Anam Hospital1 site in 1 country170 target enrollmentStarted: August 1, 2015Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
170
Locations
1
Primary Endpoint
optimal laryngeal mask airway cuff volume

Study Overview

Brief Summary

Overinflation of laryngeal mask airway cuff increase side effect like hoarseness, vocal cord paralysis, sorethroat. The investigators will study correlation between laryngeal mask airway cuff volume and pressure and physical examination of head and neck.

Detailed Description

Overinflation of laryngeal mask airway cuff can induce side effects like hoarseness, vocal cord paralysis, sorethroat. Some study revealed that 60cmH2O of intracuff pressure is maximum pressure which is not increase side effect.

The manufacturer recommends that the cuff is inflated with the minimum volume of air required to provide an effective seal(max volume - size 3, 20 ml; size 4, 30 ml; size 5, 40).

The investigators will measure anatomical structure (neck circumference, neck length, thyroid-mental distance, etc.) which can influence cuff volume and pressure and find correlation between cuff volume and physical figure measured.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Screening
Masking
None

Eligibility Criteria

Ages
19 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Adult (age 19-65)
  • American Society of Anesthesiology Classification I-III

Exclusion Criteria

  • cardiovascular disease, cerebrovascular disease, pulmonary disease
  • patient who have operation history for airway
  • patient who expected difficult intubation
  • patient who have risk of aspiration

Arms & Interventions

Classic laryngeal mask airway

Other

single arm

Intervention: Classic laryngeal mask airway (Device)

Outcomes

Primary Outcomes

optimal laryngeal mask airway cuff volume

Time Frame: 20minutes

◦The investigators remove air until gas leak occured around the cuff under airway pressure 15cm H20, fresh gas flow 6liters/min. Check the volume and pressure just before leakage occured.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Hye-Won Shin

Director, MD, PhD

Korea University Anam Hospital

Study Sites (1)

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