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GlideScope® vs GlideScope® + aScope® for Managing Difficult Airways.

GlideScope® vs GlideScope® + aScope® for Managing Difficult Airways. Assessment of a New Procedure for Endotracheal Intubation in Patients With Suspected Difficult Airways

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02627755
Enrollment
160
Registered
2015-12-11
Start date
2016-11-21
Completion date
2017-11-21
Last updated
2017-02-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Airway Morbidity, Anesthesia Intubation Complication

Keywords

videolaryngoscopy, difficult airway management

Brief summary

The use in a combined way of two systems of intubation (Glidescope + aScope) would condition an increase in the success rate of endotracheal intubation maneuver compared to conventional isolated Glidescope use in patients with clinical criteria of difficult airway.

Detailed description

Worldwide, up to 600 patients are estimated to die annually as a result of the complications that occur during tracheal intubation The GlideScope® (videolaryngoscope) is used for endotracheal intubation in patients with difficult airway predictors, in this patients overall success intubation rate is 96%. but success intubation rate at first attempt is only 86%. Despite this positive rates, due to high comorbidity when intubation fails, both failure rates (inverse of success rate) are impermissible. 14% failure at the first attempt intubation as well as 4% overall intubation failure. in this study the investigators try to show that new procedure associating aScope® (disposable fiberscope) together with GlideScope® increases the success intubation rate of both ( overall and first attempt).

Interventions

DEVICEaScope®

we use the aScope® as a flexible and dirigible guide to facilitate the passage of the endotracheal tube through the vocal cords.

use of Glidescope® in conventional manner to facilitate endotracheal intubation

Sponsors

Instituto de Investigacion Sanitaria La Fe
CollaboratorOTHER
Hospital de Manises
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients programed for general anesthesia with endotracheal intubation required that presents one or both criteria of difficult airway predictors: * criteria 1: Arne test \>10 (Arne J,1998) * criteria 2: Ratio between neck circumference and thyromental distance \> 4. (Kim WH, 2011)

Exclusion criteria

* Patients with mouth opening which does not allow the introduction of video laryngoscope. * Patients with indication of flexible fiberoptic intubation with awake patient.

Design outcomes

Primary

MeasureTime frameDescription
first attempt intubation success ratethrough study completion, an average of 1 year.first attempt intubation success rate

Secondary

MeasureTime frameDescription
overall intubation success ratethrough study completion, an average of 1 year.through study completion, an average of 1 year.
intubation time (in seconds)through study completion, an average of 1 yearduring anesthetic induction time until inflate pneumo tamponade after tracheal intubation
complications related to intubation30 days postoperativequestionnaire

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026