MedTrace Logo

Double Lumen Tube Intubation

NCT02295657 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2014-11-20

No results posted yet for this study

Summary

The aim of this study was to compare time, success rates of different double-lumen tubes in intubation in a standardized manikin model.

Conditions

  • Endotracheal Intubation
  • Cardiac Arrest

Interventions

DEVICE

standard double-lumen tube

intubation using standard double-lumen tube

DEVICE

VivaSight Double Lumen Tube

intubation using VivaSight Double Lumen Tube

Sponsors & Collaborators

  • International Institute of Rescue Research and Education

    lead OTHER

Principal Investigators

  • Lukasz Szarpak · Institute of Cardiology

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-11-30
Primary Completion
2014-12-31
Completion
2014-12-31

Countries

  • Poland

Study Locations

More Related Trials

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 NCT02295657 on ClinicalTrials.gov