COPD Aerosol Study Comparing the Efficacy of Nebulizers Versus Dry Powder Inhalers

NACompletedINTERVENTIONAL
Enrollment

7

Participants

Timeline

Start Date

February 28, 2015

Primary Completion Date

March 31, 2016

Study Completion Date

March 31, 2016

Conditions
COPD Exacerbation
Interventions
DRUG

Formoterol

Comparison of dosage administered via a nebulizer versus dosage administered via a dry powder inhaler. 12 µg Formoterol with the dry powder inhaler and 20 µg (solution form) of Formoterol with the nebulizer. Patients will receive formoterol and placebo at both study visit #1 and visit #2.

OTHER

Placebo

Comparison of drug administered via a nebulizer versus a dry powder inhaler. The placebo used will be sterile, preservative free, normal saline for inhalation for the nebulizer and a matched capsule without active drug for the dry powder inhaler. All patients will receive 2 ml of normal saline with the nebulizer to match the volume of nebulized formoterol solution. Patients will receive formoterol and placebo at both study visit #1 and visit #2.

Trial Locations (1)

37920

University of Tennessee Medical Center, Knoxville

All Listed Sponsors
collaborator

Mylan Specialty L.P.

UNKNOWN

lead

University of Tennessee Graduate School of Medicine

OTHER

NCT02291016 - COPD Aerosol Study Comparing the Efficacy of Nebulizers Versus Dry Powder Inhalers | Biotech Hunter | Biotech Hunter