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Macintosh Versus GlideScope Versus C-MAC for Double Lumen Endotracheal Intubation

NCT05091281 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 105

Last updated 2022-01-12

No results posted yet for this study

Summary

The double lumen endotracheal tube (DLT) is the most widely-used device for single lung ventilation in current thoracic anesthesia practice. In recent years, the routine application of the videolaryngoscope for single lumen endotracheal intubation has increased; nevertheless there are few studies of the use of the videolaryngoscope for DLT. The authors wondered whether there were benefits to using the videolaryngoscope for DLT placement in patients with predicted normal airways. Therefore, this study was designed to compare the performances of the GlideScope®, the C-MAC®(D) videolaryngoscope and the Macintosh laryngoscope in DLT intubation.

Conditions

  • Thoracic

Interventions

DEVICE

Intubation of the double lumen tube by Macintoch laryngoscope

After induction of anesthesia insertion of the double lumen tube was done by Macintosh laryngoscope

DEVICE

Intubation of the double lumen tube by Glidescope videolaryngoscope

After induction of anesthesia insertion of the double lumen tube was done by GlideScope® videolaryngoscope

DEVICE

Intubation of the double lumen tube by C-MAC®(D) videolaryngoscope

After induction of anesthesia insertion of the double lumen tube was done by C-MAC®(D) videolaryngoscope

Sponsors & Collaborators

  • Tanta University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-11-05
Primary Completion
2022-01-10
Completion
2022-01-10

Countries

  • Egypt

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 NCT05091281 on ClinicalTrials.gov