Clinical Trials Directory

Trials / Completed

CompletedNCT03094806

Vibratory PEP Device and Hospital Length of Stay for Acute Exacerbation of COPD

Vibratory/Positive Expiratory Pressure Device and Hospital Length of Stay for Acute Exacerbation of Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
91 (actual)
Sponsor
New York Presbyterian Brooklyn Methodist Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is evaluating the use of a respiratory device, the Acapella Vibratory Positive Expiratory Pressure (PEP) Therapy device, in patients admitted to the hospital with a chronic obstructive pulmonary disease (COPD) exacerbation.

Detailed description

The investigators hypothesize that the PEP-FV used as adjunctive therapy in patients hospitalized for an acute exacerbation of COPD will result in decreased hospital length of stay and improvement of overall COPD-related health outcomes.

Conditions

Interventions

TypeNameDescription
DEVICEAcapella Vibratory PEP Therapy Device plus usual careThe acapella® Vibratory PEP Therapy System (PEP-FV) device is a handheld device that operates in same principle as standard FV. Unlike standard FV, it is not gravity dependent. It comes in two different devices to accommodate for different flows rates of the patient. It has similar properties of a standard FV and may be better tolerated.
DEVICESham Acapella Vibratory PEP Device plus usual careThe Sham Acapella Vibratory PEP Device is the same as the Therapy Device, except the flutter valve has been removed from the device.

Timeline

Start date
2013-10-01
Primary completion
2015-10-01
Completion
2015-12-01
First posted
2017-03-29
Last updated
2024-03-21
Results posted
2018-10-11

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT03094806. Inclusion in this directory is not an endorsement.