Clinical Trials Directory

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

TypeNameDescription
DRUGarformoterol15 mcg administered via nebulizer
DRUGsalmeterol50 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.