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NIS for Patients Using Symbicort Turbuhaler for Maintenance and Reliever Therapy in a Single Inhaler (SYMCO)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
ClinicalTrials.gov Identifier: NCT00557297
Recruitment Status : Completed
First Posted : November 14, 2007
Last Update Posted : September 25, 2008
Sponsor:
Information provided by:

Study Description
Brief Summary:
The aim of this non-interventional study is to ensure that patients in routine clinical practice follow given treatment instructions and to evaluate the number of reliever inhalations as well as the number of patient/days with more than 8/12 total inhalations at any day. If the number of reliever inhalations and thus the received inhaled glucocorticosteroid dose is not excessive, the safety conclusions from the clinical studies can be extrapolated to real life for better acceptance of SMART (Symbicort Maintenance and Reliever Therapy).

Condition or disease
Asthma

Study Design

Study Type : Observational
Estimated Enrollment : 250 participants
Time Perspective: Cross-Sectional
Official Title: NIS for Patients Using Symbicort Turbuhaler for Maintenance and Reliever Therapy in a Single Inhaler
Study Start Date : October 2007
Study Completion Date : September 2008
Groups and Cohorts


Outcome Measures

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Persistent asthma
  • Prior Symbicort Turbuhaler maintenance and reliever therapy in a single inhaler
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00557297


Locations
Latvia
Research Site
Aluksne, Latvia
Research Site
Aozkraukle, Latvia
Research Site
Balvi, Latvia
Research Site
Cesis, Latvia
Research Site
Gulbene, Latvia
Research Site
Jekabpils, Latvia
Research Site
Jumprava, Latvia
Research Site
Kekava, Latvia
Research Site
Kraslava, Latvia
Research Site
Kuldiga, Latvia
Research Site
Liepaja, Latvia
Research Site
Limbazi, Latvia
Research Site
Livani, Latvia
Research Site
Madona, Latvia
Research Site
Ogre, Latvia
Research Site
Preili, Latvia
Research Site
Rezekne, Latvia
Research Site
Salacgriva, Latvia
Research Site
Saldus, Latvia
Research Site
Talsi, Latvia
Research Site
Valniera, Latvia
Research Site
Ventspils, Latvia
Sponsors and Collaborators
AstraZeneca
More Information

ClinicalTrials.gov Identifier: NCT00557297     History of Changes
Other Study ID Numbers: D5890L00031
First Posted: November 14, 2007    Key Record Dates
Last Update Posted: September 25, 2008
Last Verified: September 2008

Keywords provided by AstraZeneca:
asthma
SMART
inhaled
glucocorticosteroid
reliever
maintenance
single inhaler

Additional relevant MeSH terms:
Budesonide, Formoterol Fumarate Drug Combination
Anti-Asthmatic Agents
Respiratory System Agents