Status:

COMPLETED

A Cross-sectional Study of COPD and Symptom Variability in MEA Countries

Lead Sponsor:

AstraZeneca

Conditions:

Chronic Obstructive Pulmonary Disease

Eligibility:

All Genders

Brief Summary

This non-interventional study aims at assessing stable GOLD C and D COPD patient's perception of daily and weekly symptoms variability and their impact on daily activities. It will also explore the c...

Detailed Description

1. Primary objective: To assess perception of daily and weekly variability of symptoms in stable GOLD C and D COPD patients and their impact on daily life activities 2. Secondary objectives: * To ...

Eligibility Criteria

Inclusion

  • Patients eligible for inclusion have to fulfill all of the following criteria:
  • Stable GOLD C or D COPD patient under maintenance treatment, over 45 years, who provided signed informed consent;
  • COPD diagnosis documented by spirometry performed in the past 12 months with an FEV1/FVC \< 0.7 and an FEV1 \< 50% predicted.

Exclusion

  • Patients are not eligible for inclusion if they meet one of the following criteria:
  • Patient with an ongoing COPD exacerbation\*;
  • Patient who has experienced an exacerbation\* in the previous 3 months;
  • History of asthma, allergic rhinitis, lung cancer or any other significant respiratory disease, such as tuberculosis, lung fibrosis or sarcoidosis;
  • Inability to understand the study related questions;
  • Mentally disabled patient or unable to read and write;
  • Pregnant.
  • Current participation in a clinical trial;

Key Trial Info

Start Date :

December 7 2015

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 31 2017

Estimated Enrollment :

3254 Patients enrolled

Trial Details

Trial ID

NCT03425760

Start Date

December 7 2015

End Date

March 31 2017

Last Update

June 29 2018

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