Symbicort Turbuhaler 30/60 Clinical Experience Investigation
NCT ID: NCT01232348
Last Updated: 2011-12-07
Study Results
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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COMPLETED
3643 participants
OBSERVATIONAL
2010-01-31
2011-10-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Symbicort
Those with an exposure
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
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AstraZeneca
INDUSTRY
Responsible Party
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Principal Investigators
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Yoshida Shigeru, MD
Role: STUDY_DIRECTOR
AstraZeneca
Locations
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Research Site
Okazaki, Aichi-ken, Japan
Research Site
Akita, Akita, Japan
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Aomori, Aomori, Japan
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Chiba, Chiba, Japan
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Ehime, Ehime, Japan
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Fukui-shi, Fukui, Japan
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Fukuoka, Fukuoka, Japan
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Fukushima, Fukushima, Japan
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Gifu, Gifu, Japan
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Gunma, Gunma, Japan
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Hiroshima, Hiroshima, Japan
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Hokkaido, Hokkaido, Japan
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Hyogo, Hyōgo, Japan
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Ibaraki, Ibaraki, Japan
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Ishikawa, Ishikawa-ken, Japan
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Numakunai, Iwate, Japan
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Kagawa, Kagawa-ken, Japan
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Kagoshima, Kagoshima-ken, Japan
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Kanagawa, Kanagawa, Japan
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Kochi, Kochi, Japan
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Kumamoto, Kumamoto, Japan
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Kyoto, Kyoto, Japan
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Miemachi, Mie-ken, Japan
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Miyagi, Miyagi, Japan
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Miyazaki, Miyazaki, Japan
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Nagano, Nagano, Japan
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Nagasaki, Nagasaki, Japan
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Nara, Nara, Japan
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Niigata, Niigata, Japan
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Ōita, Oita Prefecture, Japan
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Okayama, Okayama-ken, Japan
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Okinawa, Okinawa, Japan
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Osaka, Osaka, Japan
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Saga, Saga-ken, Japan
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Saitama, Saitama, Japan
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Shiga, Shiga, Japan
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Shimane, Shimane, Japan
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Shizuoka, Shizuoka, Japan
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Tochigi, Tochigi, Japan
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Tokushima, Tokushima, Japan
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Tokyo, Tokyo, Japan
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Tottori-shi, Tottori, Japan
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Toyama, Toyama, Japan
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Wakayama, Wakayama, Japan
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Yamagata, Yamagata, Japan
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Yamaguchi, Yamaguchi, Japan
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Yamanashi, Yamanashi, Japan
Countries
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Other Identifiers
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D589IL00001
Identifier Type: -
Identifier Source: org_study_id