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Ambu® Aura-ITM Versus Ambu Aura GainTM for Fiberoptic Intubation in Children

NCT03411655 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60

Last updated 2018-01-26

No results posted yet for this study

Summary

The investigators test the hypothesis that fiberoptic intubation (time and success rate) differ between the Ambu® Aura-ITM and Ambu Aura GainTM in paralyzed anaesthetized pediatric patients

Conditions

  • Anesthesia

Interventions

DEVICE

Ambu Aura GainTM

Time and success rate

DEVICE

Ambu® Aura-ITM

Time and success rate

Sponsors & Collaborators

  • Medical University Innsbruck

    collaborator OTHER

  • Schulthess Klinik

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Months
Max Age
6 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-03-31
Primary Completion
2018-06-30
Completion
2018-08-31

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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 NCT03411655 on ClinicalTrials.gov