Comparison of McGrath Series 5 and Airtraq Videolaryngoscope for Double-lumen Tube (DLT) Intubation

NCT ID: NCT02329041

Last Updated: 2017-04-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-01-31

Study Completion Date

2016-05-31

Brief Summary

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Previous study showed that McGrath Series 5 videolaryngoscope is an alternative tool for double-lumen tube intubation. We have compared it with traditional Macintosh laryngoscopefor double-lumen tube intubation. In this study, we will investigate its role in double-lumen tube intubation by comparison with another videolarygoscope.

Detailed Description

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The investigators designed a randomised controlled study to compare of McGrath Series 5 and Airtraq videolaryngoscope for DLT intubation in intubation time and the first attempt success rate.

Conditions

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Intubation;Difficult Thoracic Disease Intubation Complication

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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McGrath Series 5

DLT intubation with McGrath Series 5 videolaryngoscope

Group Type EXPERIMENTAL

McGrath Series 5

Intervention Type DEVICE

one kind of videolaryngoscopes, which are widely used in airway management.

Airtraq

DLT intubation with Airtraq videolaryngoscope

Group Type ACTIVE_COMPARATOR

Airtraq

Intervention Type DEVICE

another kind of videolaryngoscopes, which are also widely used in airway management.

Interventions

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McGrath Series 5

one kind of videolaryngoscopes, which are widely used in airway management.

Intervention Type DEVICE

Airtraq

another kind of videolaryngoscopes, which are also widely used in airway management.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Adult patients
* Thoracic surgery required one lung ventilation

Exclusion Criteria

* ASA physical status \>4
* Emergent operation
* planned tracheotomy
* difficult intubation predicted by a simplified airway risk index score
Minimum Eligible Age

18 Years

Maximum Eligible Age

70 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Huazhong University of Science and Technology

OTHER

Sponsor Role lead

Responsible Party

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Wenlong Yao

M.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Yuke Tian, M.D.

Role: STUDY_CHAIR

[email protected]

Locations

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Tongji Hospital, Huazhong University of Science and Technology

Wuhan, Hubei, China

Site Status

Countries

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China

Other Identifiers

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TJMZK201412002

Identifier Type: -

Identifier Source: org_study_id

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