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SYMBICORT® in the Treatment of COPD (SRP COPD)

AstraZeneca logo

AstraZeneca

Status

Completed

Conditions

COPD

Study type

Observational

Funder types

Industry

Identifiers

NCT00564499
SRP-RB-COPD-2005/1

Details and patient eligibility

About

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

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • patients who recently quit smoking (<3months)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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