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

NCT02745964 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 8

Last updated 2018-07-18

No results posted yet for this study

Summary

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

Conditions

  • General Anesthesia

Interventions

DEVICE

LMA supreme

Anesthesia is maintained using LMA supreme in LMA supreme group or using I-gel in I-gel group according to the randomly allocated groups.

DEVICE

I-gel

Anesthesia is maintained using LMA supreme in LMA supreme group or using I-gel in I-gel group according to the randomly allocated groups.

Sponsors & Collaborators

  • Yonsei University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-05-09
Primary Completion
2016-06-11
Completion
2016-06-11

Countries

  • South Korea

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02745964 on ClinicalTrials.gov