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Pre Hospital Evaluation of Video Laryngoscopy

NCT01374061 · Status: WITHDRAWN · Phase: PHASE4 · Type: INTERVENTIONAL

Last updated 2014-05-08

No results posted yet for this study

Summary

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

Conditions

  • Cardiac Arrest
  • Respiratory Distress Syndrome
  • Shock
  • Acute Post-trauma Stress State
  • Drug Toxicity
  • Trauma, Nervous System

Interventions

DEVICE

Classical intubation

Classical intubation

DEVICE

GLIDESCOPE

GLIDESCOPE intubation

Sponsors & Collaborators

  • Ministry of Health, France

    collaborator OTHER_GOV

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Sébastien GALLULA, Ph · Assistance Publique - Hôpitaux de Paris

  • Patrick PLAISANCE, MD, PhD · Assistance Publique - Hôpitaux de Paris

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-06-30
Primary Completion
2012-12-31
Completion
2012-12-31

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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 NCT01374061 on ClinicalTrials.gov