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SYMBICORT® in the Treatment of COPD

A Scientific Research Program to Evaluate the Efficacy of SYMBICORT® 320/9μg in the Treatment of COPD in Real Life Environment by General Practitioners

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00564499
Acronym
SRP COPD
Enrollment
Unknown
Registered
2007-11-28
Start date
2006-03-31
Completion date
2007-05-31
Last updated
2011-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD

Keywords

COPD, Symbicort, General Practitioners

Brief summary

A Scientific Research Program to evaluate the efficacy of SYMBICORT® 320/9μg in the treatment of COPD in real life environment by General Practitioners

Interventions

None listed

Sponsors

AstraZeneca
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CROSSOVER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients (m/f) with COPD (GOLD stadium III and IV)

Exclusion criteria

* patients who recently quit smoking (\<3months)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026