Asthma Clinical Trial
Official title:
Utilization Patterns of Pulmicort HFA in Real Life Practice
| Verified date | November 2010 |
| Source | AstraZeneca |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | Spain: Spanish Agency of Medicines |
| Study type | Observational |
The purpose of this study is to identify the potential issues during short and mid term utilization of Pulmicort hydro fluoroaklane (HFA) pressurized metered-dose inhaler (pMDI)and describe associated factors.
| Status | Completed |
| Enrollment | 260 |
| Est. completion date | February 2009 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | N/A and older |
| Eligibility |
Inclusion Criteria: - Asthmatic patients with a diagnose of at least 12 months of duration before study inclusion - Patients previously treated with Pulmicort CFC who have changed their treatment to Pulmicort HFA Exclusion Criteria: - Disability that, from investigator point of view, prevent from complying the follow up schedule - To have participated in any clinical study in the past 6 months |
Observational Model: Cohort, Time Perspective: Prospective
| Country | Name | City | State |
|---|---|---|---|
| Spain | Research Site | Alcorcon | Madrid |
| Spain | Research Site | Barcelona | |
| Spain | Research Site | Fuentes de Ebro | Zaragoza |
| Spain | Research Site | Leganes | Madrid |
| Spain | Research Site | Madrid | |
| Spain | Research Site | Murcia | |
| Spain | Research Site | Olivares | Sevilla |
| Spain | Research Site | Sabadell | Barcelona |
| Spain | Research Site | San Sebastian de los Reyes | Madrid |
| Spain | Research Site | Toledo |
| Lead Sponsor | Collaborator |
|---|---|
| AstraZeneca |
Spain,
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