Skip to content

Biannual Review of Exhaled Air and Trends in Health Evaluation in COPD

Biannual Review of Exhaled Air and Trends in Health Evaluation in COPD

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07045948
Acronym
BREATHE-COPD
Enrollment
100
Registered
2025-07-01
Start date
2025-07-14
Completion date
2028-06-30
Last updated
2025-09-11

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

Conditions

COPD

Keywords

FeNO, Blood eosinophil count, COPD

Brief summary

This study aims to evaluate how airway inflammation, lung function, and symptoms change over time in people with chronic obstructive pulmonary disease (COPD). Airway inflammation will be assessed using a simple breath test (FeNO) and a small blood sample to measure eosinophils, a type of white blood cell. Participants will be followed for one year, with three study visits (at the start, 6 months, and 12 months). The goal is to understand how these markers evolve and whether they differ between people who experience a worsening of symptoms (called exacerbations) and those who remain stable. All tests except for a small extra blood draw are part of routine COPD care. Participation does not affect standard treatment.

Interventions

DIAGNOSTIC_TESTBlood eosinophil Count

Blood sample for blood eosinophil count

Sponsors

Universitair Ziekenhuis Brussel
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged ≥ 40 years * Diagnosed with COPD according to GOLD criteria * Attending routine follow-up visits every 6 months * Ability to provide informed consent

Exclusion criteria

* Recent respiratory tract infection or exacerbation (either moderate or se-vere) (\<4 weeks before inclusion) * Dominant asthmatic phenotype (ACO with asthma predominance) * Severe comorbidities interfering with participation or follow-up

Design outcomes

Primary

MeasureTime frame
To evaluate the longitudinal stability of FeNO levels in COPD patients over a 12-month period with biannual measurements.from enrollment to the end of the study period (1 year)

Countries

Belgium

Contacts

Primary ContactNaomi Michotte, MD
pneumologie@uzbrussel.be024776841

Outcome results

None listed

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