Intubation Clinical Trial
Official title:
A Prospective Comparison of the Glidescope Cobalt to Standard Direct Laryngoscopy in Infants
The investigators seek to prospectively compare intubation with the Glidescope Cobalt to Direct Laryngoscopy (DL) in infants.
Status | Completed |
Enrollment | 66 |
Est. completion date | March 2012 |
Est. primary completion date | February 2011 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | N/A to 1 Year |
Eligibility |
Inclusion Criteria: 1. Scheduled to undergo elective surgery at CHOP 2. American Society of Anesthesiologists (ASA) Physical Status I or II 3. Anesthetic plan requiring tracheal intubation with a neuromuscular relaxant 4. Parental/guardian permission (informed consent). Subjects will be too young to understand the study procedures and therefore assent will not be sought. - Exclusion Criteria: 1. At known or anticipated high risk for aspiration pneumonia 2. Known or predicted difficult intubation as assessed by the clinical attending anesthesiologist 3. Emergency surgical procedure 4. Patients with preoperative airway pathology or stridor - |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | The Children's Hospital of Philadelphia | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
Children's Hospital of Philadelphia |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time to Tracheal Intubation | The amount of time it takes the anesthesiologist to insert a breathing tube using one of two methods, either by direct laryngoscopy or using the Glidescope Cobalt Video system. | Measured the time of the randomized device past the teeth/gums until its removal after intubation as the time to intubation. | No |
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