N/A Completed N=66 Randomized Treatment

Comparing Use of the Glidescope Cobalt to Direct Laryngoscopy in Infants

Intubation

Source: ClinicalTrials.gov NCT01163656 ↗

Enrolled (actual)

Serious AEs

—

Results posted

Jan 2013

Primary outcomePrimary: Time to Tracheal Intubation — 21.4; 22.6 seconds

Summary

The investigators seek to prospectively compare intubation with the Glidescope Cobalt to Direct Laryngoscopy (DL) in infants.

Outcome Measures

Outcome	Result	p-value
PRIMARY Time to Tracheal Intubation	21.4; 22.6	—

Eligibility Criteria

Inclusion Criteria

Scheduled to undergo elective surgery at CHOP
American Society of Anesthesiologists (ASA) Physical Status I or II
Anesthetic plan requiring tracheal intubation with a neuromuscular relaxant
Parental/guardian permission (informed consent). Subjects will be too young to understand the study procedures and therefore assent will not be sought. -

Exclusion Criteria

At known or anticipated high risk for aspiration pneumonia
Known or predicted difficult intubation as assessed by the clinical attending anesthesiologist
Emergency surgical procedure
Patients with preoperative airway pathology or stridor -

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01163656). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.