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Evaluation of the Ambu ® aScope® for Tracheal Intubation in Difficult Airways

NCT01467739 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2013-12-16

No results posted yet for this study

Summary

The purpose of this study is to evaluate a disposable fiberscope (Ambu ® aScope®) for tracheal intubation in difficult airways due to cervical immobilization by a cervical collar, and compare it to a conventional reusable fiberscope.

Conditions

  • Surgical Intervention
  • Endotracheal Intubation

Interventions

DEVICE

Ambu ® aScope®

DEVICE

a conventional reusable fiberscope

Sponsors & Collaborators

  • University of Lausanne Hospitals

    lead OTHER

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2011-11-30
Completion
2011-11-30

Countries

  • Switzerland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01467739 on ClinicalTrials.gov