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

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

Asthma

Study type

Observational

Funder types

Industry

Identifiers

NCT00557297
D5890L00031

Details and patient eligibility

About

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).

Enrollment

250 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

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

Trial contacts and locations

22

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Data sourced from clinicaltrials.gov

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