Symbicort SMART (Symbicort Maintenance And Reliever Therapy)

NCT ID: NCT00523679

Last Updated: 2009-07-13

Study Results

Results pending

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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Recruitment Status

COMPLETED

Total Enrollment

2000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-07-31

Study Completion Date

2008-07-31

Brief Summary

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The purpose of this study is to investigate the extent of Symbicort use in patients prescribed Symbicort as maintenance and reliever therapy.

Detailed Description

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Conditions

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Asthma

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Asthma patients prescribed Symbicort as maintenance and reliever therapy, according to the label, before inclusion in this program.
Minimum Eligible Age

12 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Principal Investigators

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Joon-Woo Bahn

Role: STUDY_DIRECTOR

AstraZeneca Korea

Locations

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Research Site

Seoul, Jongro-gu, South Korea

Site Status

Research Site

Seoul, Kangnam-gu, South Korea

Site Status

Research Site

Seoul, Songpa-gu, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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NIS-RKR-SYM-2007/1

Identifier Type: -

Identifier Source: org_study_id

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