Symbicort Maintenance and Reliever Therapy - Experience in Real Life Setting in Malaysia

NCT00576316 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 201

Last updated 2010-12-16

Study results available
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Summary

The purpose of the study is to evaluate the satisfaction level of patients using the Symbicort SMART approach for their asthma management.

Conditions

Interventions

DRUG

Symbicort Turbuhaler 160/4.5

Sponsors & Collaborators

Principal Investigators

  • Akhmal Yusof, MD · AstraZeneca

  • Aziah Ahmad Mahayiddin, MD · Kuala Lumpur Hospital

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-01-31
Completion
2008-11-30

Countries

  • Malaysia

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00576316 on ClinicalTrials.gov