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Assessment of Preoxygenation Strategies in the Prehospital Environment

NCT02694705 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-09-30

No results posted yet for this study

Summary

Comparison of the preoxygenation efficacy of tidal volume breathing using three different preoxygenation techniques which are available to providers in the prehospital environment.

Conditions

Interventions

DEVICE

Continuous Positive Airway Pressure (CPAP)

CPAP provided by a portable Draeger Oxylog® 3000 plus ventilator

DEVICE

Bag-Valve-Mask (BVM)

Preoxygenation provided by BVM device, oxygen flow rate 15 l/min

DEVICE

Non-rebreather Mask (NRM)

Preoxygenation provided by NRM, oxygen flow rate 15 l/min

Sponsors & Collaborators

  • Essex and Herts Air Ambulance

    collaborator OTHER

  • Queen Mary University of London

    lead OTHER

Principal Investigators

  • Christopher J Groombridge, MBBS · Queen Mary University of London

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2016-02-29
Primary Completion
2016-07-31
Completion
2016-07-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

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 NCT02694705 on ClinicalTrials.gov