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SHARE - Symbicort and Health Economics in a Real Life Evaluation

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 3

Conditions

Asthma

Treatments

Drug: Budesonide
Drug: Terbutaline
Drug: Formoterol

Study type

Interventional

Funder types

Industry

Identifiers

NCT00259766
D5890L00001
SHARE

Details and patient eligibility

About

The purpose of this study is to compare health-related costs and asthma control in ordinary clinical practice during 12 months for Symbicort® given as a low maintenance dose plus as needed compared to a free combination of Pulmicortâ and Oxis® plus Bricanyl® as needed, and Symbicort fixed dosing plus Bricanyl as needed in asthmatic patients not adequately controlled on inhaled glucocorticosteroids alone.

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Signed informed consent,
  • asthma,
  • previously treated with glucocorticosteroids and B2-agonist

Exclusion criteria

  • History of smoking, pregnancy, any significant disease or disorder which may put the patient at risk because of study participation

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

Trial contacts and locations

108

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Data sourced from clinicaltrials.gov

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