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
| Type | Name | Description |
|---|---|---|
| DEVICE | Acapella Vibratory PEP Therapy Device plus usual care | The 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. |
| DEVICE | Sham Acapella Vibratory PEP Device plus usual care | The 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.