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Cross-over Comparison of the V60 System to Other Bi-Level Noninvasive Ventilators

NCT00817804 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 3

Last updated 2009-08-19

Study results available
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Summary

The purpose of this study is to compare a new noninvasive ventilator to existing ventilators already used for patient care.

Conditions

Interventions

DEVICE

Use of the V60 Mask Ventilator

The V60 Mask Ventilator used to provide noninvasive ventilation. It is compared to the patient's conventional ventilator in a cross-over study. The ventilator settings can range from CPAP to Pressure Support ventilation with values of IPAP and EPAP to match the conventional ventilation on which the patient had been placed.

Sponsors & Collaborators

  • Respironics, California, Inc.

    lead INDUSTRY

Principal Investigators

  • Steven Mink, MD · University of Manitoba, Winnipeg, Manitoba, Canada

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
7 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2009-03-31
Completion
2009-03-31

Countries

  • Canada

Study Locations

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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 NCT00817804 on ClinicalTrials.gov