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Clinical Trials/EUCTR2009-015876-86-GB
EUCTR2009-015876-86-GB
Active, not recruiting
Not Applicable

An investigation into the mechanisms of action of a combined long acting beta agonist/inhaled corticosteroid (Seretide 500 accuhaler) on the bacterial colonisation, immunology and inflammation of patients with Chronic Obstructive Pulmonary Disease (COPD) - An investigation of the mechanism of action of Seretide in COPD

Southampton University Hospitals0 sitesMarch 29, 2010

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Not specified
Sponsor
Southampton University Hospitals
Status
Active, not recruiting
Last Updated
13 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 29, 2010
End Date
TBD
Last Updated
13 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
All

Investigators

Sponsor
Southampton University Hospitals

Eligibility Criteria

Inclusion Criteria

  • COPD will be defined as forced expiratory volume in one second (FEV1\) of \<80% predicted for age and height, and salbutamol reversibility of \<400 ml with airflow obstruction evidenced by a ratio of FEV1 to forced vital capacity (FVC) of \<70%. A minimum of a 10 pack year history in all groups. Healthy smokers will be subjects who have smoked a minimum of 10 pack years but have normal lung function, they will be matched in all other criteria to the COPD patients. Mild, moderate and severe patients will be defined by FEV1\. Mild \>50\-80% Moderate \>30%\-50% Severe \<30% The COPD patients are to have never used components present in the Seretide (Salmeterol and flixotide)
  • Are the trial subjects under 18? no
  • Number of subjects for this age range: 0
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 0
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 0

Exclusion Criteria

  • Patients with a history of asthma, bronchiectasis, carcinoma of the bronchus, or other significant respiratory disease will be excluded. A comprehensive history, chest x\-ray and reversibility studies performed on this cohort will be used to identify those with other lung pathology. Patients will also be excluded if they have exacerbated during the last 6 weeks. Patients will also be excluded if they have been prescribed inhaled corticosteroids for the treatment of their condition.

Outcomes

Primary Outcomes

Not specified

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