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Comparison of McGrath and Macintosh Laryngoscope for DLT Intubation

NCT ID: NCT02190201

Last Updated: 2014-11-21

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

PHASE4

Total Enrollment

114 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-07-31

Study Completion Date

2014-11-30

Brief Summary

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The investigators previous study showed that McGrath Series 5 videolaryngoscope is an alternative tool for double-lumen tube intubation. But it is not determined about the advantages and disadvantages of McGrath Series 5 videolaryngoscope for double-lumen tube intubation, compared with traditional Macintosh laryngoscope.

Detailed Description

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The investigators designed a randomised controlled study to compare of McGrath Series 5 videolaryngoscope and Macintosh laryngoscope for DLT intubation.

Conditions

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Intubation; Difficult Thoracic Diseases 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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videolaryngoscope

DLT intubation with McGrath videolaryngoscope

Group Type EXPERIMENTAL

videolaryngoscope

Intervention Type DEVICE

a kind of videolaryngoscopes, which are widely used in difficult airways.

Direct laryngoscope

DLT intubation with Macintosh laryngoscope

Group Type ACTIVE_COMPARATOR

Direct laryngoscope

Intervention Type DEVICE

A kind of traditional laryngoscopes

Interventions

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videolaryngoscope

a kind of videolaryngoscopes, which are widely used in difficult airways.

Intervention Type DEVICE

Direct laryngoscope

A kind of traditional laryngoscopes

Intervention Type DEVICE

Other Intervention Names

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McGrath series 5 videolaryngoscope Macintosh laryngoscopes

Eligibility Criteria

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Inclusion Criteria

* Adult patients
* Thoracic surgery required one lung ventilation

Exclusion Criteria

* Difficult ventilation
* Emergent operation
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

Huazhong University of Science and Technology

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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TJMZK201405001

Identifier Type: -

Identifier Source: org_study_id