Study to Assess the Effect of the Aerobika Device in Addition to Standard of Care Treatment in Sputum Producing COPD Patients Using FRI

PHASE4CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

December 31, 2016

Primary Completion Date

August 31, 2017

Study Completion Date

August 31, 2017

Conditions
Pulmonary Disease, Chronic ObstructiveCOPD
Interventions
DEVICE

Aerobika® Device

For a period of 15 +/- 3 days subjects will use the Aerobika® device before administration of their stable standard of care treatment regimen (i.e. study patients should use the device before each inhalation medication administration, with a minimum use of the device of twice daily).

RADIATION

HRCT scans

A HRCT scan at Functional Residual Capacity (FRC) and Total Lung Capacity (TLC) will be taken on visit 1, and visit 3. An upper airway (UA) scan will be taken on visit 1.

Trial Locations (1)

2650

University Hospital of Antwerp, Edegem

Sponsors

Lead Sponsor

All Listed Sponsors
lead

FLUIDDA nv

INDUSTRY