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Video Laryngoscope, New Intubation Device

Advanced Video Laryngoscope, a New Practical Intubation Device: Randomized Clinical Trial in 401 Patients

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02095470
Enrollment
401
Registered
2014-03-24
Start date
2013-02-28
Completion date
2014-02-28
Last updated
2014-03-24

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

Conditions

Elective Intubation

Keywords

Laryngoscopy, Equipment, Video Laryngoscope

Brief summary

new glidoscope was tested on 401 patients

Detailed description

Four hundred and one patients who were scheduled for elective operation, were randomly assigned to be intubated by direct laryngoscopy using a Macintosh blade size 3rd (DL, n=196) or intubation using the video laryngoscope (VL, n=205). Prior to intubation all patients were given a similar regimen of induction of anesthesia. The patients were then intubated, using direct laryngoscopy or the VL, by a different anesthetist during which the larynx was inspected and given a laryngoscopy score. Time to intubate, failure rate, injuries, personnel pleasure and, aspiration rate were measured

Interventions

newly developed innovatory device

DEVICEtraditional laryngoscope

traditional way for intubation

Sponsors

Education Development Center, Inc.
CollaboratorINDUSTRY
Shiraz University of Medical Sciences
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
19 Years to 68 Years
Healthy volunteers
Yes

Inclusion criteria

* elective operation who filled the consent

Exclusion criteria

* poor intubation * emergency cases * hemodynamic derangement

Design outcomes

Primary

MeasureTime frameDescription
laryngoscopy gradehospital stay (average 48 hours)grade of laryngoscopy
time to intubation60 minutestime to successful intubation in minutes
unsuccessful attempts60 minutesnumber of failure

Secondary

MeasureTime frameDescription
aspirationhospital stay ( 48 hours)clinical aspiration or radiological

Countries

Iran

Outcome results

None listed

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