Trial Outcomes & Findings for Comparison of GlideScope-Specific Rigid Stylet to Standard Malleable Stylet for GlideScope Intubation by Novice Operators (NCT NCT00884754)

NCT ID: NCT00884754

Last Updated: 2011-01-11

Results Overview

Recruitment status

COMPLETED

Study phase

NA

Target enrollment

60 participants

Primary outcome timeframe

30-150 seconds (anticipated)

Results posted on

2011-01-11

Participant Flow

Participant milestones

Participant milestones
Measure
Rigid GlideScope Specific Stylet
90º Curvature, Malleable Stylet
Overall Study
STARTED
30
30
Overall Study
COMPLETED
30
30
Overall Study
NOT COMPLETED
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Comparison of GlideScope-Specific Rigid Stylet to Standard Malleable Stylet for GlideScope Intubation by Novice Operators

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Rigid GlideScope Specific Stylet
n=30 Participants
90º Curvature, Malleable Stylet
n=30 Participants
Total
n=60 Participants
Total of all reporting groups
Age Categorical
Over 18 years
30 participants
n=5 Participants
30 participants
n=7 Participants
60 participants
n=5 Participants
Sex: Female, Male
Female
15 Participants
n=5 Participants
18 Participants
n=7 Participants
33 Participants
n=5 Participants
Sex: Female, Male
Male
15 Participants
n=5 Participants
12 Participants
n=7 Participants
27 Participants
n=5 Participants

PRIMARY outcome

Timeframe: 30-150 seconds (anticipated)

Outcome measures

Outcome measures
Measure
Rigid GlideScope Specific Stylet
n=30 Participants
90º Curvature, Malleable Stylet
n=30 Participants
Time to Intubation (Seconds)
60 seconds
Interval 48.0 to 75.0
61 seconds
Interval 49.0 to 75.0

Adverse Events

Rigid GlideScope Specific Stylet

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

90º Curvature, Malleable Stylet

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

Philip Jones

London Health Sciences Centre

Phone: 519-685-8500

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place