Trials / Completed
CompletedNCT01391559
Efficacy of Inhaling Bronchodilator Medications in Chronic Obstructive Pulmonary Disease
Efficacy of Inhaling Bronchodilator Medications in Patients With Chronic Obstructive Pulmonary Disease Who Have a Low Peak Inspiratory Flow Rate
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 20 (actual)
- Sponsor
- Dartmouth-Hitchcock Medical Center · Academic / Other
- Sex
- All
- Age
- 60 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
Some patients with Chronic Obstructive Pulmonary Disease (COPD) report that they are uncertain whether they achieve clinical benefit using a dry-powder inhaler (DPI). One possible explanation is that the patient is unable to inhale the dry powder bronchodilator medication into the lower respiratory tract due to a low peak inspiratory flow rate (PIFR). A PIFR \< 60 l/min is considered to be suboptimal flow for a DPI, including the Diskus device. The hypothesis of the study is that the forced expiratory volume in 1 second (FEV1) measured at two hours after inhalation of the study medication will be higher with arformoterol solution (15 mcg) from a nebulizer compared with salmeterol dry powder (50 mcg) inhaled from the Diskus.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | arformoterol | 15 mcg administered via nebulizer |
| DRUG | salmeterol | 50 mcg delivered vis Diskus |
Timeline
- Start date
- 2011-07-01
- Primary completion
- 2012-10-01
- Completion
- 2012-10-01
- First posted
- 2011-07-12
- Last updated
- 2013-08-07
- Results posted
- 2013-08-07
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT01391559. Inclusion in this directory is not an endorsement.