Skip to main content
Clinical Trials/NCT00972491
NCT00972491CompletedNot Applicable

The Optimal Time of Insertion of Laryngeal Mask Airway With Propofol Induction

Tufts Medical Center1 site in 1 country198 target enrollmentStarted: September 1, 2009Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
198
Locations
1
Primary Endpoint
Ease of Mouth opening

Study Overview

Brief Summary

Laryngeal mask airway (LMA) is routinely used for some patients who have surgery under general anesthesia. LMA is placed in the mouth and allow the anesthesia to be given without having to put a breathing tube in the throat. Previous studies have focused on the effect of different anesthesia medicines on optimal condition for LMA use. The objective of the present study is to find the optimal time for LMA insertion.

Detailed Description

This is a randomized, controlled, blinded trial. Midazolam, 2 mg and fentanyl 1.0 µg/kg, would be given prior to induction with propofol, 2.5 mg/kg.

The investigator who does the induction of general anesthesia will also be responsible for the timekeeping. For this reason, it is not possible for this investigator to be blinded to randomization. The induction would conclude after loss of eyelash reflex (LER). At that point insertion of the LMA (#4 for females, #5 for males) will occur 0, 60 and 90 seconds after LER. The LMA will be lubricated with a water soluble gel and will be inserted with a deflated cuff according to the technique described by Brain.

The investigator who inserts the LMA (Inv1) will be in the operating room and blinded to randomization groups by not seeing the induction of general anesthesia. This investigator will insert the LMA only when called by the investigator who induces general anesthesia (Inv2). Inv1 will also grade ease of LMA insertion.

The primary outcome is Jaw opening at the time of LMA insertion, defined as full 1, partial 2, and nil 3.

Secondary outcomes include:

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Outcomes Assessor)

Eligibility Criteria

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

Inclusion Criteria

  • •subjects 18 years or older
  • •ASA status 1-3

Exclusion Criteria

  • •high risk of aspiration
  • •anticipated difficult airway
  • •use of sedative drugs
  • •patient refusal

Arms & Interventions

0 sec, 60 sec, 90 sec

Other

LMA will be inserted at 0, 60, and 90 seconds after eyelash reflex disappears

Intervention: Insertion of Laryngeal Mask Airway (Procedure)

Outcomes

Primary Outcomes

Ease of Mouth opening

Time Frame: From Induction of general anesthesia to satisfactory LMA insertion

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

Loading locations...

Similar Trials