NL-OMON39121
Completed
Not Applicable
Assessment of Comorbidities in COPD in European Symptomatic Subjects from primary care. - ACCESS
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- COPD
- Sponsor
- GlaxoSmithKline
- Enrollment
- 480
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Males/females \>\= 40 years of age.
- •2\. COPD (all GOLD\-stages) diagnosed \>\= 12 months ago.
- •3\. FEV1/FVC (tiffeneau\-index) after use of bronchodilator \< 0\.70\.
- •4\. Smoking history of \>\= 10 packyears
- •5\. Singed informed consent form.
Exclusion Criteria
- •1\.In the opinion of the investigator, there is a current primary diagnosis of asthma (patients with a primary diagnosis of COPD but who also have asthma may be included)
- •2\.A diagnosis of fibrosis or asbestosis
- •3\.Diagnosis of cancer \- includes current and within the last 5 years (patients in remission for \>\= 5 years may be included). Patients diagnosed with cancer during the study will be withdrawn
- •4\.Diagnosis of clinically significant bronchiectasis
- •5\.Subjects who are concurrently participating in any clinical study or who have received any investigational drugs within 4 weeks of Visit 1, or who will start any during the study period.
- •6\.Unable to or unwilling to conform with the study requirements including completion of the health status questionnaires
- •7\.Females who are pregnant or lactating.
Outcomes
Primary Outcomes
Not specified
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