Utilization Patterns of Pulmicort in Real Life Practice
NCT ID: NCT00660569
Last Updated: 2010-12-01
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
260 participants
OBSERVATIONAL
2008-01-31
2009-02-28
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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1
Asthmatic patients with a diagnose of at least 12 months of duration before study inclusion, previously treated with Pulmicort chlorofluorocarbons (CFC) who have changed their treatment to Pulmicort HFA
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patients previously treated with Pulmicort CFC who have changed their treatment to Pulmicort HFA
Exclusion Criteria
* To have participated in any clinical study in the past 6 months
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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AstraZeneca
Principal Investigators
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Javier Nuevo Rivero
Role: STUDY_DIRECTOR
AstraZeneca MC SpainEpidemiologyValue Demonstration Unit
Locations
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Research Site
Barcelona, Barcelona, Spain
Research Site
Sabadell, Barcelona, Spain
Research Site
Alcorcón, Madrid, Spain
Research Site
Leganés, Madrid, Spain
Research Site
Madrid, Madrid, Spain
Research Site
San Sebastián de los Reyes, Madrid, Spain
Research Site
Murcia, Murcia, Spain
Research Site
Olivares, Sevilla, Spain
Research Site
Toledo, Toledo, Spain
Research Site
Fuentes de Ebro, Zaragoza, Spain
Countries
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Other Identifiers
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NIS-RES-PUL-2007/1
Identifier Type: -
Identifier Source: org_study_id