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Budesonide/Formoterol for Maintenance and Reliever Therapy Among Asthma Patients in Thailand

Budesonide/Formoterol for Maintenance and Reliever Therapy: A Medication Use Evaluation Among Persistent Asthma Patients in General Practice in Thailand

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00800241
Enrollment
1020
Registered
2008-12-02
Start date
2009-05-31
Completion date
2009-11-30
Last updated
2010-12-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Asthma

Keywords

Asthma, Symbicort SMART, Thai patient eligibility, Persistent asthma

Brief 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.

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
12 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Number of budesonide/formoterol use per patientOn the survey date

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026