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The BASA Study: Breath Analysis for Severe Asthma Patients

A

Azienda Ospedaliera Universitaria Policlinico Paolo Giaccone Palermo

Status

Enrolling

Conditions

Severe Asthma

Treatments

Device: exhaled breath analysis

Study type

Observational

Funder types

Other

Identifiers

NCT05946421
Università di Palermo

Details and patient eligibility

About

This study will evaluate the fluctuations of exhaled breath markers in patients with severe asthma on biologics. In the study, severe asthma patients will be followed up to 16 weeks monitoring lung function and inflammation through non-invasive technologies such as exhaled breath analysis (FeNO, GC-MS and EBC). A control group will be followed up to two weeks with the overall objective to indentify and evaluate the modifcations of markers of inflammation in patient under biologic treatment.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Severe asthma diagnosis according to the latest recommendation
  • Eligible or in treatment with a biologic treatment for severe asthma
  • Able to follow istructions
  • Able and willing to sign the informed consent

Exclusion criteria

  • Not able to perform lung function measurements and the procedures of the study
  • Acute respiratory or non respiratory infection (<4 weeks)
  • Not willing to continue the study

Trial design

100 participants in 2 patient groups

Severe Asthma patients on biologics
Treatment:
Device: exhaled breath analysis
Healthy controls
Treatment:
Device: exhaled breath analysis

Trial contacts and locations

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Central trial contact

Carmen Durante; Stefania Principe, PhD

Data sourced from clinicaltrials.gov

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