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Comparison of the LMA Protector and the I-gel

Seoul National University logo

Seoul National University

Status

Completed

Conditions

Mechanical Ventilation

Treatments

Device: Laryngeal mask airway protector
Device: I-gel

Study type

Interventional

Funder types

Other

Identifiers

NCT03078517
20170104

Details and patient eligibility

About

Investigators aim to compare two supraglottic airway devices; the i-gel and the newly developed laryngeal mask airway protector in terms of airway sealing effect, the insertion success rate, and the incidence of complications in anesthetized patients.

Enrollment

110 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Requirement for mechanical ventilation under general anesthesia

Exclusion criteria

  • Surgical position other than supine position
  • Tumors or anatomical abnormalities in the upper airway
  • Known or predicted difficult airway
  • Body mass index > 30 kg/m2
  • Required postoperative mechanical ventilation
  • Head and neck surgery
  • Aspiration tendency

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

110 participants in 2 patient groups

I-gel group
Active Comparator group
Description:
After the induction of anesthesia, I-gel is inserted into the oropharyngeal space.
Treatment:
Device: I-gel
LMA protector group
Experimental group
Description:
After the induction of anesthesia, laryngeal mask airway protector is inserted into the oropharyngeal space.
Treatment:
Device: Laryngeal mask airway protector

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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