Evaluation of Airtraq in Pediatric

November 18, 2009 updated by: King Khaled Eye Specialist Hospital

Evaluation of Airtraq in Pediatric Population: A Prospective Randomized Study

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

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

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

Study Type

Interventional

Enrollment (Anticipated)

50

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Riyadh, Saudi Arabia, 11462
        • King Khaled Eye Specialist Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

2 years to 10 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

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.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Airtraq group
Use Airtraq for intubation
intubation with airtraq
Other Names:
  • Optical laryngoscope
Active Comparator: Macintoch gorup
Use Macintoch laryngoscope for intubation
use Macintoch laryngoscope for intubation
Other Names:
  • Standard laryngoscope

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Duration of intubation
Time Frame: two minutes
two minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Waleed Riad, MD, AB, SB, King Khaled Eye Specialist Hospital

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

April 1, 2009

Primary Completion (Actual)

November 1, 2009

Study Completion (Actual)

November 1, 2009

Study Registration Dates

First Submitted

June 9, 2009

First Submitted That Met QC Criteria

June 9, 2009

First Posted (Estimate)

June 10, 2009

Study Record Updates

Last Update Posted (Estimate)

November 19, 2009

Last Update Submitted That Met QC Criteria

November 18, 2009

Last Verified

November 1, 2009

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • RP 0909

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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