Asthma Control-A "Patient Follow up Programme" Maintenance and Reliever Therapy in a Single Inhaler

NCT ID: NCT00524641

Last Updated: 2009-07-09

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

1254 participants

Study Classification

OBSERVATIONAL

Study Start Date

2007-07-31

Study Completion Date

2008-04-30

Brief Summary

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To investigate the change in patient's asthma symptom control using ACQ scores after 4 to 6 weeks of Symbicort Turbuhaler (budesonide/ formoterol) in SMART approach.

Detailed Description

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Conditions

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Asthma

Study Design

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Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Asthma patients from both sexes, age 18 or older
* Have already been on Symbicort SMART treatment
* Willing to give written informed consents to participate in the program.

Exclusion Criteria

* Patients who are not willing to give written informed consent
* Patients in emergency care for asthma at ICUs or COPD patients are excluded from the program.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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AstraZeneca

INDUSTRY

Sponsor Role lead

Principal Investigators

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Dinh Ngoc SY, MD

Role: STUDY_CHAIR

TB and Lung Disease Hospital, Hanoi

Tran Van Ngoc, MD, PhD

Role: STUDY_CHAIR

Cho Ray Hospital

Nguyen Hong Duc

Role: STUDY_CHAIR

Pharm Ngoc Thach Hospital

Do Van Dung, MD, PhD

Role: STUDY_CHAIR

Ho Chi Minh City Univ of Medicine and Pharmacist

Locations

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Research Site

Hanoi, , Vietnam

Site Status

Research Site

Ho Chi Minh City, , Vietnam

Site Status

Countries

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Vietnam

Other Identifiers

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NIS-R84-AST-2007/3

Identifier Type: -

Identifier Source: secondary_id

NIS-RVN-SYM-2007/1

Identifier Type: -

Identifier Source: org_study_id

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