Comparing Bronchodilation of Symbicort With and Without Valved Holding Chamber (Aerochamber Plus) (WSMR2)
Asthma
About this trial
This is an interventional other trial for Asthma focused on measuring Asthma, Formoterol, Long Acting Beta Adrenergic Bronchodilator, Symbicort, Aerochamber
Eligibility Criteria
Inclusion Criteria:
- Asthma with 15% or more increase in Forced expiratory volume at 1 second (FEV-1) after 180-360 mcg of albuterol pMDI
Exclusion Criteria:
- Any illness or condition which might place subject at risk in the study;e.g. some cardiovascular disorders Inability to understand and sign informed consent
Sites / Locations
- Western Sky Medical Research
Arms of the Study
Arm 1
Arm 2
Other
Experimental
Group 1 / use of pMDI as approved
Group 2 / pMDI with Aerochamber Plus
The intervention in this group will use inhalation from the pMDI containing budesonide/formoterol pMDI 160/4.5 2 inhalations as approved. (FDA approved product information) without a spacer. The pulmonary function tests (PFTs) will be collected at baseline and for a period of 12 hours post inhalation of 2 inhalation of budesonide /formoterol; pMDI160/5.
The intervention in this group will use the pMDI budesonide/formoterol 160/4.5 with a valve holding chamber spacer device, Aerochamber Plus which is the intervention being studied The PFTs will be collected at baseline and for a period of 12 hours post inhalation of 2 inhalation of Symbicort 160/5. This is the intervention to be studied for comparison to the non-spacer inhalations..