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Incidence of Sore Throat With Traditional Intubation Blades or Glidescope Blade

NCT02033564 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 151

Last updated 2014-01-13

No results posted yet for this study

Summary

The purpose in this study is to determine whether there is a difference in the incidence of postoperative sore throat when using the GlideScope™ versus a traditional intubation blade involving patients that are not anticipated to have a difficult airway.

Conditions

  • Intratracheal Intubation
  • Laryngoscopes
  • Postoperative Care
  • Risk Assessment

Interventions

DEVICE

Macintosh/Miller Laryngoscope

DEVICE

Glidescope Laryngoscope

Sponsors & Collaborators

  • Albany Medical College

    collaborator OTHER

  • Jason Ngo, B.S.

    lead OTHER

Principal Investigators

  • Dennis J Cirilla, DO · Department of Anesthesiology, Albany Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-06-30
Primary Completion
2013-03-31
Completion
2013-03-31

Countries

  • United States

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 NCT02033564 on ClinicalTrials.gov