Comparison of Lighted Stylet and GlideScope for Double-lumen Endobronchial Intubation

NCT ID: NCT03514745

Last Updated: 2018-07-03

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

80 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-05-06

Study Completion Date

2019-05-31

Brief Summary

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We evaluate the GlideScope and lighted stylet for DLT intubation in terms of the intubation time, number of intubation attempts, difficulty in DLT advancement towards the glottis, postoperative sore throat and hoarseness, and hemodynamic responses during intubation in patients with predicted difficult airways.

Detailed Description

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Conditions

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Intubation;Difficult

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

TRIPLE

Participants Caregivers Outcome Assessors

Study Groups

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GlideScope group

After the induction of anesthesia, endobronchial intubation is performed using the GlideScope.

Group Type ACTIVE_COMPARATOR

GlideScope

Intervention Type DEVICE

Endobronchial intubation is performed using the GlideScope.

Lighted stylet group

After the induction of anesthesia, endobronchial intubation is performed using a lighted stylet.

Group Type EXPERIMENTAL

Lighted stylet

Intervention Type DEVICE

Endobronchial intubation is performed using a lighted stylet.

Interventions

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GlideScope

Endobronchial intubation is performed using the GlideScope.

Intervention Type DEVICE

Lighted stylet

Endobronchial intubation is performed using a lighted stylet.

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* adult patients undergoing thoracic surgery requiring endobronchial intubation for one-lung ventilation

Exclusion Criteria

* presence of sore throat and hoarseness
* requirements for postoperative mechanical ventilation
* at risk of aspiration.
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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SMG-SNU Boramae Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Jin-Young Hwang

MD.PhD.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Jin-Young Hwang, M.D., Ph.D.

Role: STUDY_DIRECTOR

Seoul Metropolitan Government Seoup National University Boramae Medical Center

Locations

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Seoul Metropolitan Government Seoul National University Boramae Medical Center

Seoul, , South Korea

Site Status RECRUITING

Countries

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South Korea

Central Contacts

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Jin-Young Hwang, M.D., Ph.D.

Role: CONTACT

82-2-870-2518

Facility Contacts

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Jin-Young Hwang, M.D.

Role: primary

+82-2-870-2518

Other Identifiers

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20171227

Identifier Type: -

Identifier Source: org_study_id

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