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The Depth of Endotracheal Tube Insertion

NCT ID: NCT03184246

Last Updated: 2018-12-06

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

100 participants

Study Classification

INTERVENTIONAL

Study Start Date

2017-06-30

Study Completion Date

2018-12-04

Brief Summary

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The investigators suppose that direct laryngoscopy is connected with deeper insertion of endotracheal tube in comparison to videolaryngoscopy. Correction of this malposition can cause postoperative discomfort and further complications in some patients.Routine use of videolaryngoscopy could minimize these problems.

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Detailed Description

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100 patients scheduled for elective neurosurgical procedures will be randomized into two groups. Patients in group A will be intubated by videolaryngoscopy (GlideScope), patients in group B by direct laryngoscopy, in both groups will be rigid stylet used. Intubation will be done under propofol anesthesia, targeted entropy 40 to 50, and deep relaxation (neuromuscular transmission target level 0). Sufentanil will be used to block tracheal reflexes. In both groups the depth of insertion of tracheal tube will be measured in the mouth corner immediately after intubation. Next day, the unpleasant sensations and complications will be recorded (sore throat, stridor, hoarseness, cough and nausea and vomiting) during control visit of patients.

Conditions

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Intubation Complication

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Interventional group will be intubated by videolaryngoscopy, control group by direct laryngoscopy
Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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GlideScope

intubation with GlideScope

Group Type EXPERIMENTAL

GlideScope

Intervention Type DEVICE

videolaryngoscopy (GlideScope) will be used for intubation

Direct laryngoscopy

intubation with laryngoscope

Group Type ACTIVE_COMPARATOR

Direct laryngoscopy

Intervention Type DEVICE

direct laryngoscopy will be used for intubation

Interventions

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GlideScope

videolaryngoscopy (GlideScope) will be used for intubation

Intervention Type DEVICE

Direct laryngoscopy

direct laryngoscopy will be used for intubation

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* American Society of Anesthesiologists physical status I - III

Exclusion Criteria

* postoperative ventilation, laryngeal tumors, conditions after tracheotomy or laryngeal operations, cervical spinal hernia extraction
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital Hradec Kralove

OTHER

Sponsor Role lead

Responsible Party

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Dostalova Vlasta, MD, PhD

MD, Ph.D.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Pavel Dostal, MD, Ph.D.

Role: STUDY_DIRECTOR

University Hospital Hradec Kralove

Locations

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University Hospital Hradec Kralove

Hradec Králové, , Czechia

Site Status

Countries

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Czechia

Other Identifiers

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University Hospital

Identifier Type: -

Identifier Source: org_study_id

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