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OpenTrials
Completed

NCT Number: NCT00946452

Symbicort SMART Satisfaction From Patient Perspective 2009

To characterize the level of asthma control and patient satisfaction amongst diagnosed asthma sufferers who are currently receiving Symbicort Maintenance and Reliever Therapy (SMART) in Malaysia.

Completed

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Key information

Age range

18 year–59 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Research Site

Petaling Jaya, Selangor, Malaysia

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have been prescribed Symbicort SMART (1 or 2 inhalation twice daily) by their Dr's for the past 3 months
  • Informed consent

Exclusion criteria

  • Symbicort SMART treatment < 3 months
  • Patients requiring short courses of oral steroids more than twice in a month

Treatment and study plan

Primary outcomes

  1. Score level of Satisfaction in Asthma Treatment Questionnaire (SATQ)

    Time frame: After 3 months on SMART - once

  2. Score level of Asthma Control Test (ACT)

    Time frame: After 3 months on SMART - once

Sponsors and collaborators

Lead sponsor

AstraZeneca

Industry

Registry information

Important dates

Study start
2009
Primary completion
2010
Study completion
2010
First posted
Jul 27, 2009
Registry last updated
Mar 18, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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