Observational Study on Efficacy of Alvesco(Ciclesonide) in Asthma Children and Adolescent in Real Practice

NCT ID: NCT01438255

Last Updated: 2012-08-23

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

274 participants

Study Classification

OBSERVATIONAL

Study Start Date

2010-07-31

Brief Summary

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This is a prospective, non-comparative, open, observational study.

Detailed Description

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Conditions

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Asthma

Study Design

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Study Time Perspective

PROSPECTIVE

Study Groups

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Alvesco

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Children who is prescribed with ciclesonide for asthma

Exclusion Criteria

* Subjects with contraindications to ciclesonide use
* Subjects with clinically relevant concomitant disease that could compromise the patient's safety should not be included in this study.
Minimum Eligible Age

6 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Handok Inc.

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Handok Pharmaceuticals

Seoul, Seoul, South Korea

Site Status

Countries

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South Korea

Other Identifiers

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ALVESCO-OS01

Identifier Type: -

Identifier Source: org_study_id