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Video Laryngoscope, New Intubation Device

S

Shiraz University of Medical Sciences

Status and phase

Completed
Phase 3
Phase 2

Conditions

Elective Intubation

Treatments

Device: traditional laryngoscope
Device: video laryngoscope

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02095470
93-4687 (Other Identifier)
93-4678

Details and patient eligibility

About

new glidoscope was tested on 401 patients

Full 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

Enrollment

401 patients

Sex

All

Ages

19 to 68 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • elective operation who filled the consent

Exclusion criteria

  • poor intubation
  • emergency cases
  • hemodynamic derangement

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

401 participants in 2 patient groups, including a placebo group

videolaryngoscope group
Experimental group
Description:
video laryngoscopy was done for them
Treatment:
Device: video laryngoscope
traditional laryngoscope
Placebo Comparator group
Description:
comparison to active group with routine laryngoscope
Treatment:
Device: traditional laryngoscope

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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