Now Available for Public Comment: Notice of Proposed Rulemaking (NPRM) for FDAAA 801 and NIH Draft Reporting Policy for NIH-Funded Trials

Evaluation of Airtraq in Pediatric

This study has been completed.
Sponsor:
Information provided by:
King Khaled Eye Specialist Hospital
ClinicalTrials.gov Identifier:
NCT00917566
First received: June 9, 2009
Last updated: November 18, 2009
Last verified: November 2009

June 9, 2009
November 18, 2009
April 2009
November 2009   (final data collection date for primary outcome measure)
Duration of intubation [ Time Frame: two minutes ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00917566 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
Not Provided
Not Provided
 
Evaluation of Airtraq in Pediatric
Evaluation of Airtraq in Pediatric Population: A Prospective Randomized Study

This study indented to evaluate the use of Optical laryngoscope in pediatric

The authors are welling to study how intubation will differ if Airtraq optical laryngoscope used in pediatrics

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Subject)
Primary Purpose: Treatment
Intubation
  • Device: Airtraq
    intubation with airtraq
    Other Name: Optical laryngoscope
  • Device: Macintoch
    use Macintoch laryngoscope for intubation
    Other Name: Standard laryngoscope
  • Active Comparator: Airtraq group
    Use Airtraq for intubation
    Intervention: Device: Airtraq
  • Active Comparator: Macintoch gorup
    Use Macintoch laryngoscope for intubation
    Intervention: Device: Macintoch
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
50
November 2009
November 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Healthy children undergoing general anesthesia required tracheal intubation.

Exclusion Criteria:

  • History of difficult intubation.
  • Risk of aspiration.
  • Children with cardiovascular disease.
  • Children with respiratory disease.
Both
2 Years to 10 Years
No
Contact information is only displayed when the study is recruiting subjects
Saudi Arabia
 
NCT00917566
RP 0909
Yes
Waleed Riad, King khaled Eye specialist hospital
King Khaled Eye Specialist Hospital
Not Provided
Principal Investigator: Waleed Riad, MD, AB, SB King Khaled Eye Specialist Hospital
King Khaled Eye Specialist Hospital
November 2009

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP