MedTrace Logo

Wearable Noninvasive Positive Pressure Ventilation Device in COPD

NCT03130361 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2018-10-03

No results posted yet for this study

Summary

The objective is to assess the impact of a wearable Noninvasive Positive Pressure Ventilation, on physical activity and quality of life in patients with severe COPD, complaining of dyspnea.

Conditions

  • Non-Invasive Ventilation

Interventions

DEVICE

Non-Invasive Ventilation

Sponsors & Collaborators

  • Philips Respironics

    collaborator INDUSTRY

  • Icadom

    lead INDUSTRY

Principal Investigators

  • Jean-Louis PEPIN, Pr · Laboratoire du sommeil - Centre hospitalier Universitaire Michallon - 38043 GRENOBLE

Study Design

Allocation
NA
Purpose
DEVICE_FEASIBILITY
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2017-01-12
Primary Completion
2018-01-10
Completion
2018-01-10

Countries

  • France

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 NCT03130361 on ClinicalTrials.gov