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Clinical Trials/NCT01374061
NCT01374061
Withdrawn
Phase 4

Pre Hospital Evaluation of Video Laryngoscopy : a Comparative Study of Macintosh and GLIDESCOPE Ranger®

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Cardiac Arrest
Sponsor
Assistance Publique - Hôpitaux de Paris
Primary Endpoint
IDS score in each group
Status
Withdrawn
Last Updated
11 years ago

Overview

Brief Summary

The objective of this work is to compare standard intubation with video laryngoscope (Glide scope Ranger ) in French pre hospital multicentric study.

Detailed Description

Introduction: In France, patients in critical status brought to hospital by emergency physicians and nurses experimented in tracheal intubation. It is an invasive act allowing a protection of airways and an optimal oxygenation of the patients in distress. The reference technique is the direct laryngoscopy by Macintosh . Corresponding data shows that a video laryngoscope - GLIDESCOPE laryngoscope - improve the conditions of intubation in the surgical unit thanks to a better display(visualization) of the opening. A derived device for pre hospital emergency units (GLIDESCOPE Ranger®) deserves to be compared with the classic laryngoscopy in emergency conditions. Objectives: compare the emergency intubation in Pre hospital meadow by Glide Scope Ranger with regard to the classic method Progress of the study: the patients will be included by emergency physicians working in out of hospital teams of 3 major hospitals of Paris. The patients will be randomized in 2 groups: 1 group classic laryngoscopy (group 1) and a group Glide scope Ranger (group 2). The score IDS will be compared for every group as well as the arisen of a complication during the procedure. The consent will be collected on the place or during the hospitalization.

Registry
clinicaltrials.gov
Start Date
June 2011
End Date
December 2012
Last Updated
11 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • patients of more than 18 years old
  • requiring an intubation
  • by medical out of hospital emergency operators
  • medical insurance
  • Consent signed

Exclusion Criteria

  • Age \<18, pregnant women
  • Refusal of consent or inability for understanding study
  • small mouth opening makes it impossible intubate

Outcomes

Primary Outcomes

IDS score in each group

Time Frame: during the intubation

Secondary Outcomes

  • Hemodynamic instability(per intubation)
  • Vomit / regurgitation or inhalation per-procedure(during the intubation)
  • Dental or throat traumatism(during the intubation)
  • Broncho/laryngospasm(during the intubation)
  • Hypoxia(per intubation)
  • Inhalation pneumonia(within 24 hours following the inclusion)
  • Failure of intubate(during the intubation)

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