Stopped: Airborne particles during data collection a risk during COVID-19
This study will characterise saliva and sputum FTIR spectral profiles in patients with COPD, during exacerbations and stable disease.
Age range
40 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Disease severity
Timeframe: within a 24 month period
Disease Control
Timeframe: a change between the exacerbation visit and stable visit through study completion, an average of 2 years
FEV1 forced expiratory volume-one second
Timeframe: a change between the exacerbation visit and stable visit through study completion, an average of 2 years
FVC forced vital capacity
Timeframe: a change between the exacerbation visit and stable visit through study completion, an average of 2 years
FEV1/FVC ratio
Timeframe: a change between the exacerbation visit and stable visit through study completion, an average of 2 years
Sputum Culture
Timeframe: immediately during analysis