A Follow-up Programme for Patients Using Symbicort SMART in Normal Clinical Practice

AstraZeneca

Status: Completed

Conditions: Bronchial Asthma

Study type: Observational

Funder types: Industry

Identifiers

NCT00505388

D5890C00018

EuDract 2006-005677-22

Details and patient eligibility

About

This patient follow-up programme was designed to describe the extent of Symbicort use in patients prescribed Symbicort as maintenance and reliever therapy in routine clinical practice in comparison with the already documented use of Symbicort as maintenance and reliever therapy in clinical therapies

Enrollment: 5,137 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Asthma patients prescribed Symbicort as maintenance and reliever therapy, according to the label, before inclusion in this programme
• signed and dated informed consent(ICF)
• for patients under-age, signed and dated ICF form from both the patient and the patient's parent/legal guardian is required

Exclusion criteria

• Involvement in the planning and conduct of the programme (applies to both AstraZeneca staff or staff at the investigational site)