airway obstruction COPD
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Study 1;COPD patients: •Adults between 40-65 years •Lungfunction: FEV1/VC10 cigarettes/day, >10 packyears) Controls: •Adults between 40-65 years •Healthy with a negative history on lung diseases or any other illness. •Prebronchodilator FEV1 > 80% predicted, FEV1/FVC > 0.70 (22) •Actual smoker(>10 cigarettes/day, > 10 packyears);Study 2;COPD patients: •Adults between 40-65 years •Lungfunction: FEV1/VC 1 year, > 10 packyears) Controls: •Adults between 40-65 years •Healthy with a negative history on lung diseases or any other illness. •Prebronchodilator FEV1 > 80% predicted, FEV1/FVC > 0.70 (22) •Actual non-smoker(> 1 year);Study 3;COPD patients: •Adults between 40-65 years •Lungfunction: FEV1/VC1 year, > 10 packyears) Asthma patients: •Adults between 40-65 years •episodic chest symptoms, documented reversibility in FEV1 by 400 µg inhaled salbutamol > 12 %pred or airway hyperresponsiveness (PC20 methacholine 1 year,
Exclusion criteria
Exclusion criteria: •Other pulmonary diseases •Pregnancy •Diabetes mellitus (documented in the past) •Hypercholesterolaemia (documented in the past) •Exacerbation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Study 1: the change in smellprint before and after smoking a cigarette. Study 2: the change in smellprint before, during and after oxygen supply Study 3: the change in smellprint before and after nebulisation of salbutamol/ipratropiumbromide | — |
Countries
Netherlands