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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00800241
Other study ID # NIS-RTH-SYM-2008/1
Secondary ID
Status Completed
Phase N/A
First received December 1, 2008
Last updated December 2, 2010
Start date May 2009
Est. completion date November 2009

Study information

Verified date December 2010
Source AstraZeneca
Contact n/a
Is FDA regulated No
Health authority Thailand: Ethical Committee
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the incidence of misuse, i.e., over-use and under-use, of Budesonide/formoterol for maintenance and reliever therapy in usual-care setting.


Recruitment information / eligibility

Status Completed
Enrollment 1020
Est. completion date November 2009
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 12 Years and older
Eligibility Inclusion Criteria:

- Established persistent asthma

- Currently treated with Symbicort SMART for 3 months or longer

Exclusion Criteria:

- currently participating or have participated in a study with an investigational compound within the last 30 days

- current diagnosis of chronic obstructive pulmonary disease (COPD)

- smoked more than 10 pack-year

Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


Locations

Country Name City State
Thailand Research Site Buriram
Thailand Research Site Chanthaburi
Thailand Research Site Chiang Mai
Thailand Research Site Mahasarakham
Thailand Research Site Nakhon Phanom
Thailand Research Site Nakhon Srithammarat
Thailand Research Site Nakhonpathom
Thailand Research Site Phattalung
Thailand Research Site Phitsanulok
Thailand Research Site Rayong
Thailand Research Site Roi Et
Thailand Research Site Samutsakhon
Thailand Research Site Surat Thani
Thailand Research Site Trang

Sponsors (1)

Lead Sponsor Collaborator
AstraZeneca

Country where clinical trial is conducted

Thailand, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of budesonide/formoterol use per patient On the survey date No
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