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

NCT00817297 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2017-11-17

No results posted yet for this study

Summary

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

Conditions

Interventions

DEVICE

noninvasive ventilator

Experimental V60 Mask noninvasive Ventilator for treating patients with COPD, then Comparator Conventional Mask noninvasive Ventilator for treating patients with COPD in crossover study design

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
SINGLE
Model
CROSSOVER

Eligibility

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

Timeline & Regulatory

Start
2009-01-17
Primary Completion
2009-03-03
Completion
2009-04-07

Countries

  • Canada

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 NCT00817297 on ClinicalTrials.gov