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Markers for Chronic Obstructive Pulmonary Disease (COPD)

Imperial College London logo

Imperial College London

Status

Withdrawn

Conditions

Current Smokers
COPD Patients
Healthy Non-smokers

Treatments

Procedure: St Georges Questionnaire
Procedure: Blood test
Procedure: CT Scan
Procedure: Exhaled Breath Condensate
Procedure: Bodypletysmography
Procedure: Induced Sputum
Procedure: Spirometry
Procedure: Exhaled Nitric Oxide and Carbon Monoxide

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT00180622
SD-000-068

Details and patient eligibility

About

The primary aim of this study is to exploit a difference between COPD patients, chronic smokers without COPD and healthy non-smoking subjects. This will help to assess the utility of inflammatory and oxidative markers in exhaled air and sputum and to compare them with the lung function, clinical parameters and computerised tomography (CT).

Sex

All

Ages

30 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy non-smokers

  • FEV1 >80% predicted
  • FEV1 reversibility of <10% after inhaled (beta2-agonists

Current smokers

  • FEV1 no less than 80% predicted
  • FEV1 reversibility of <10% after inhaled (beta2-agonists
  • Smoking history of > 10 pack-years

Moderate COPD

  • FEV1 40-59% predicted
  • FEV1 reversibility of <10% after inhaled (beta2-agonists
  • Smoking history of > 10 pack-years**

Severe COPD

  • FEV1 <40% predicted
  • FEV1 reversibility of <10% after inhaled (beta2-agonists
  • Smoking history of > 10 pack-years

Exclusion criteria

  • FEV1 increases by 200 ml and 15% of the baseline value after inhaled (beta2-agonists
  • Asthma
  • unstable disease (FEV1 <35% predicted) and/or current, or within the last 4 weeks, respiratory tract infection.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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