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Markers for Chronic Obstructive Pulmonary Disease (COPD)

Non-Invasive Markers for Chronic Obstructive Pulmonary Disease (COPD)

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00180622
Enrollment
0
Registered
2005-09-16
Start date
2001-07-01
Completion date
2002-07-01
Last updated
2019-07-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Non-smokers, Current Smokers, COPD Patients

Brief summary

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).

Interventions

PROCEDURESpirometry
PROCEDUREExhaled Nitric Oxide and Carbon Monoxide
PROCEDURECT Scan
PROCEDUREBlood test
PROCEDURESt Georges Questionnaire
PROCEDUREBodypletysmography

Sponsors

AstraZeneca
CollaboratorINDUSTRY
Imperial College London
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
Yes

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.

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026