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Non-Interventional Surveillance of Effectiveness of Symbicort® Maintenance And Reliever Therapy (Symbicort® SMART) in the Treatment of Moderate and Severe Asthma
This study is currently recruiting participants.
Verified by AstraZeneca, December 2007
Sponsored by: AstraZeneca
Information provided by: AstraZeneca
ClinicalTrials.gov Identifier: NCT00573222
  Purpose

This is a 3-month non-interventional, observational study on patients with moderate and severe asthma.


Condition Intervention
Asthma
Drug: Symbicort

MedlinePlus related topics: Asthma
Drug Information available for: Symbicort
U.S. FDA Resources
Study Type: Observational
Study Design: Prospective
Official Title: Non-Interventional Surveillance of Effectiveness of Symbicort® Maintenance And Reliever Therapy (Symbicort® SMART) in the Treatment of Moderate and Severe Asthma

Further study details as provided by AstraZeneca:

Primary Outcome Measures:
  • To evaluate & describe asthma control in adult patients w/moderate to severe asthma treated w/Symbicort SMART following the frequency, type & severity of symptoms through the Asthma Control Questionnaire.

Secondary Outcome Measures:
  • to evaluate the safety of Symbicort SMART treatment through the number and type of reported adverse events 2. assessment of patient's satisfaction with the treatment 3.assessment of physician's satisfaction with the treatment

Estimated Enrollment: 400
Study Start Date: November 2007
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with moderate and severe asthma on Symbicort SMART treatment

Exclusion Criteria:

  • Under 18 years old
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00573222

Contacts
Contact: AstraZeneca Croatia Clinical Study, Information +385 1 4628 002 Anamarija.gjurovic@strazeneca.com

Locations
Croatia
Research Site Recruiting
Zagreb, Croatia
Research Site Recruiting
Rijeka, Croatia
Research Site Recruiting
Pula, Croatia
Research Site Recruiting
Senj, Croatia
Croatia Recruiting
Zadar, Croatia
Research Site Recruiting
Sibenik, Croatia
Research Site Recruiting
Vukovar, Croatia
Research Site Recruiting
Cakovec, Croatia
Research Site Recruiting
Slavonskibrod, Croatia
Research Site Recruiting
Osijek, Croatia
Research Site Recruiting
Pozega, Croatia
Research Site Recruiting
Vinkovci, Croatia
Research Site Recruiting
Dubrovnik, Croatia
Sponsors and Collaborators
AstraZeneca
Investigators
Study Director: Anan Marija Gjurovic AstraZeneca
  More Information

Study ID Numbers: NIS-RHR-SYM-2007/1
Study First Received: December 13, 2007
Last Updated: December 13, 2007
ClinicalTrials.gov Identifier: NCT00573222  
Health Authority: Not Required:

Keywords provided by AstraZeneca:
Asthma

Study placed in the following topic categories:
Hypersensitivity
Lung Diseases, Obstructive
Symbicort
Respiratory Tract Diseases
Lung Diseases
Hypersensitivity, Immediate
Asthma
Respiratory Hypersensitivity

Additional relevant MeSH terms:
Respiratory System Agents
Immune System Diseases
Bronchial Diseases
Therapeutic Uses
Anti-Asthmatic Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 16, 2009