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Protocol for lung sample collection by bronchoscopy for laboratory research

Bronchoscopy studies in patients with asthma, chronic obstructive pulmonary disease, interstitial lung disease and healthy controls; identification of new therapeutic targets

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN63607895
Enrollment
3000
Registered
2026-03-24
Start date
2007-09-11
Completion date
Unknown
Last updated
2026-04-14

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

Conditions

Chronic obstructive pulmonary disease (COPD), asthma, interstitial lung disease (ILD) Respiratory

Interventions

Participants will undergo the following assessments for suitability for bronchoscopy: spirometry, DLCO (ILD patients only), physical examination, oxygen saturations via a pulse oximeter, blood samplin

Sponsors

Medicines Evaluation Unit
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Must be aged over 18 years, be competent to understand and give informed consent 2. Participants with asthma, COPD and ILD must have stable disease with no exacerbations or infections for at least 6 weeks prior to bronchoscopy Participants with asthma must have: 1. Clinically diagnosed asthma 2. Forced Expiratory Volume in 1 Second (FEV1) >30% predicted 3. FEV1 > 1.0 litre; participants with FEV1 >30% predicted but 30% predicted 3. FEV1 >1.0 L; participants with FEV1 >30% predicted but 35% predicted 2. Forced Vital Capacity (FVC) >45% predicted 3. Oxygen saturation above 90% on room air Healthy participants must have: 1. No history of a chronic respiratory disorder 2. No history of acute respiratory disease within 6 weeks prior to bronchoscopy 3. No other significant medical disorder that may affect the respiratory system or that causes significant disability Healthy participants who are smokers must: 1. Be current or ex-cigarette smokers with a smoking history of at least 10 pack-years 2. Have FEV1 >90% predicted Healthy participants who are non-smokers must have: No significant smoking history as judged by the investigator

Exclusion criteria

Exclusion criteria: All participants: 1. History of any other inflammatory lung condition or carcinoma of the lung 2. Participants who are taking warfarin or have any bleeding disorders 3. Women who are pregnant or breastfeeding Participants with respiratory conditions: 1. Exacerbation of disease requiring hospitalisation within previous 6 months 2. History of ITU admission secondary to asthma, COPD or ILD 3. Use of home oxygen for COPD or ILD

Countries

England, United Kingdom

Contacts

Public ContactNatalie Jackson
njackson@meu.org.uk+44 (0)1619464065

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 17, 2026