Skip to content

Analyse van uitgeademde lucht om de respons op behandeling met mepolizumab te voorspellen in patiënten met ersntig astma.

Exhaled breath analysis for prediction of response to Mepolizumab in patients with severe asthma.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON26797
Enrollment
250
Registered
2018-09-03
Start date
2016-01-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

Severe Asthma

Interventions

Niet van toepassing

Sponsors

Amsterdam UMC, University of Amsterdam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: - Adult patients with severe refractory eosinophilic asthma who are treated with Mepolizumab. -Poor asthma control or frequent (≥2 per year) exacerbations, despite high-intensity treatment while alternative diagnoses have been excluded, comorbidities are treated and compliance has been checked. -Peripheral blood eosinophil levels ≥150 cells/µl.

Exclusion criteria

Exclusion criteria: - Alcohol use <12 hours prior to measurement. - Unwillingness or inability to comply with the study protocol for any other reason.

Design outcomes

Primary

MeasureTime frame
- eNose ‘Breathprints’ (signature of mixtures of volatile organic compounds (VOCs) in exhaled breath)

Secondary

MeasureTime frame
-Absence of exacerbations during 12 months after initiation of mepolizumab therapy. -Improvement of Asthma Control Questionnaire (ACQ)-score by 0.5 points over 6 months. -Decrease of oral corticosteroid (OCS) use by 50% after 12 months. -Any switch of biological therapy.

Contacts

Public ContactA.H. Maitland-van der Zee

-

a.h.maitland@amc.nl-

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)