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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00557297
First Posted: November 14, 2007
Last Update Posted: September 25, 2008
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.
Information provided by:
AstraZeneca
  Purpose
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
Asthma

Study Type: Observational
Study Design: Time Perspective: Cross-Sectional
Official Title: NIS for Patients Using Symbicort Turbuhaler for Maintenance and Reliever Therapy in a Single Inhaler

Further study details as provided by AstraZeneca:

Estimated Enrollment: 250
Study Start Date: October 2007
Study Completion Date: September 2008
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


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 Submitted: November 9, 2007
First Posted: November 14, 2007
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