NIS for Patients Using Symbicort Turbuhaler for Maintenance and Reliever Therapy in a Single Inhaler
SYMCO
1 other identifier
observational
250
1 country
22
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).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2007
Shorter than P25 for all trials
22 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2007
CompletedFirst Submitted
Initial submission to the registry
November 9, 2007
CompletedFirst Posted
Study publicly available on registry
November 14, 2007
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2008
CompletedSeptember 25, 2008
September 1, 2008
November 9, 2007
September 24, 2008
Conditions
Keywords
Eligibility Criteria
You may qualify if:
- Persistent asthma
- Prior Symbicort Turbuhaler maintenance and reliever therapy in a single inhaler
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- AstraZenecalead
Study Sites (22)
Research Site
Alūksne, Latvia
Research Site
Aozkraukle, Latvia
Research Site
Balvi, Latvia
Research Site
Cēsis, Latvia
Research Site
Gulbene, Latvia
Research Site
Jēkabpils, Latvia
Research Site
Jumprava, Latvia
Research Site
Krāslava, Latvia
Research Site
Kuldīga, Latvia
Research Site
Ķekava, Latvia
Research Site
Liepāja, Latvia
Research Site
Limbaži, Latvia
Research Site
Līvāni, Latvia
Research Site
Madona, Latvia
Research Site
Ogre, Latvia
Research Site
Preiļi, Latvia
Research Site
Rēzekne, Latvia
Research Site
Salacgrīva, Latvia
Research Site
Saldus, Latvia
Research Site
Talsi, Latvia
Research Site
Valniera, Latvia
Research Site
Ventspils, Latvia
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
November 9, 2007
First Posted
November 14, 2007
Study Start
October 1, 2007
Study Completion
September 1, 2008
Last Updated
September 25, 2008
Record last verified: 2008-09