Inspiratory Flow Rates Achieved by the COPD Patients Through Breezhaler®, Ellipta® and Handihaler® Inhaler Devices

PHASE4CompletedINTERVENTIONAL
Enrollment

97

Participants

Timeline

Start Date

December 16, 2015

Primary Completion Date

April 29, 2016

Study Completion Date

April 29, 2016

Conditions
Pulmonary Disease, Chronic Obstructive (COPD)
Interventions
DEVICE

Breezhaler®

No active drug or placebo were administered to patients during this study. Each patient were required to inhale via all three (03) study devices (Breezhaler®, Ellipta® and Handihaler®). Each patient was required to produce at least three (03) inhalational profiles via each inhalational device, following the training and demonstration for correct inhalational procedure, for each device.

DEVICE

Ellipta®

No active drug or placebo were administered to patients during this study. Each patient were required to inhale via all three (03) study devices (Breezhaler®, Ellipta® and Handihaler®). Each patient was required to produce at least three (03) inhalational profiles via each inhalational device, following the training and demonstration for correct inhalational procedure, for each device.

DEVICE

Handihaler®

No active drug or placebo were administered to patients during this study. Each patient were required to inhale via all three (03) study devices (Breezhaler®, Ellipta® and Handihaler®). Each patient was required to produce at least three (03) inhalational profiles via each inhalational device, following the training and demonstration for correct inhalational procedure, for each device.

Trial Locations (5)

1900

Novartis Investigative Site, La Plata

7600

Novartis Investigative Site, Mar del Plata

C1426ABP

Novartis Investigative Site, CABA

B1602DQD

Novartis Investigative Site, Florida

C1425FVH

Novartis Investigative Site, Ciudad Autonoma de Bs As

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY