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A Comparison of LMA-Supreme and I-gel for the Incidence of Postoperative Sore Throat

Yonsei University logo

Yonsei University

Status

Terminated

Conditions

General Anesthesia

Treatments

Device: I-gel
Device: LMA supreme

Study type

Interventional

Funder types

Other

Identifiers

NCT02745964
4-2016-0144

Details and patient eligibility

About

The purpose of this study is to investigate and compare the incidence of the postoperative sore throat between LMA supreme and I-gel.

Enrollment

8 patients

Sex

All

Ages

19+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • adult patients aged over 19 years who are scheduled for elective surgery under general anesthesia using the laryngeal mask airway

Exclusion criteria

  • Anticipated difficult airway
  • Expected duration of surgery more than 4 hours
  • body mass index more than 35 kg/m2
  • pregnancy
  • Upper gastrointestinal surgery or open abdominal surgery.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

8 participants in 2 patient groups

LMA supreme
Experimental group
Description:
Anesthesia is maintained using LMA supreme during surgery.
Treatment:
Device: LMA supreme
I-gel
Active Comparator group
Description:
Anesthesia is maintained using I-gel during surgery.
Treatment:
Device: I-gel

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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