Asthma, COPD
Conditions
Brief summary
This study will collect sputum samples from healthy smokers, COPD smokers and COPD ex-smokers to analyse biomarkers of inflammation
Interventions
None listed
Sponsors
Babraham Institute Enterprise Limited
Respivert Ltd
Study design
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
for Healthy Smoking Subjects 1. Must have signed an informed consent indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study. 2. Be between 18 and 75 years of age, inclusive, at informed consent. 3. Healthy as determined by a physician, based on medical history and physical examination. 4. Must have smoked regularly in the 12-month period preceding the screening visit and have a pack history of ≥ 5 pack years (number of pack years = number of cigarettes per day/20 x number of years smoked). Inclusion Criteria for All COPD Subjects 1. Must have signed an informed consent indicating that they understand the purpose of and procedures required for the study and are willing to participate in the study. 2. Aged between 40 and 75 years of age inclusive, at the time of signing the informed consent. 3. COPD diagnosis: Subjects with a diagnosis of COPD as defined by the American Thoracic Society (ATS)/European Respiratory Society (ERS) guidelines (Celli, 2004). Symptoms must be compatible with COPD for at least 1 year prior to screening and post-bronchodilator spirometry readings at screening: * Post-bronchodilator FEV1/FVC ratio of \<0.7 * Post-bronchodilator FEV ≥40 % and ≤80 % of predicted normal values calculated using NHANES reference equations. Additional Inclusion for Smoking COPD Subjects 1. Must have smoked regularly in the 12-month period preceding the screening visit and have a pack history of ≥ 5 pack years (number of pack years = number of cigarettes per day/20 x number of years smoked).
Exclusion criteria
for Healthy Smoking Subjects Any potential subject who meets any of the following criteria will be excluded from the participating study. 1. Upper or lower respiratory tract infection within 4 weeks of the screening visit. 2. Positive test for alcohol at screening. 3. Taking prescription medication in the 14 days before screening. 4. Subjects whose primary consumption of tobacco is via methods other than cigarettes (manufactured or self-rolled). Primary methods of tobacco consumption that are excluded include, but are not limited to pipes, cigars and e-cigarettes. 5. Subjects who are unable to produce a total weight of at least 0.1 grams (g) of selected sputum at screening 6. Urinary cotinine levels at screening \< 30 ng/ml. 7. Subject is mentally or legally incapacitated. 8. Subject is an employee of the Sponsor or contract research organization (CRO), or a relative of an employee of the Sponsor or CRO. 9. Any other reason that the Investigator considers makes the subject unsuitable to participate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Lipid metabolites in sputum cell homogenate from healthy smokers and smokers and ex-smokers with COPD. | 8 months |
Countries
United Kingdom
Outcome results
None listed