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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00660569
Other study ID # NIS-RES-PUL-2007/1
Secondary ID
Status Completed
Phase N/A
First received April 15, 2008
Last updated November 30, 2010
Start date January 2008
Est. completion date February 2009

Study information

Verified date November 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Spain: Spanish Agency of Medicines
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

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

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Spain, 

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