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Clinical Trials/NCT03377686
NCT03377686
Completed
Not Applicable

The Feasibility and Diagnostic Value of New Point-of-care Instruments for Breath Analysis in Children With Asthma, Cystic Fibrosis (CF), and Healthy Controls

Maastricht University Medical Center1 site in 1 country56 target enrollmentMarch 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Asthma
Sponsor
Maastricht University Medical Center
Enrollment
56
Locations
1
Primary Endpoint
Number of participants with adverse events directly related to the various point-of-care tests used
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

In this study new hand-held devices for measuring exhaled breath will be tested in children with asthma, CF, and healthy controls. Main objectives will be feasibility and discriminative value of these techniques.

Detailed Description

Rationale: Assessment of volatile organic compounds (VOCs) is a new recently developed non-invasive technique to assess airway inflammation. The non-invasive character makes it highly suitable for use in (preschool) children. However, the analysis of VOCs by gas chromatography mass spectrometry technique (GC-MS), the gold standard, is expensive and time consuming. Therefore, new hand-held devices (such as electronic Noses (eNoses) and Ion Mobility Spectrometer techniques) have been developed. However, these new point-of-care instruments have not been studied in children. Objectives: 1) To test whether new point-of-care instruments for the measurement of VOCs in exhaled breath are feasible for use in children aged 6 to 16 years; 2) To explore whether these techniques can differentiate between healthy children, asthmatic children and children with Cystic Fibrosis (CF). Study design: Cross-sectional study design. Several VOCs tests will be performed in all participants.Besides, fraction of exhaled nitric oxide (FeNO) and inflammatory markers in exhaled breath condensate (EBC) will be measured. Study population: Three groups of children aged 6 to 16 years: 20 healthy children, 20 children with doctor's diagnosed asthma, 20 children with CF. Main study parameters/endpoints: Each technique will be evaluated for its use and feasibility in children. For each technique, VOC profiles between study groups will be evaluated for its discriminative power.

Registry
clinicaltrials.gov
Start Date
March 2016
End Date
December 2017
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Children aged 6 to 16 years
  • Healthy group: See exclusion criteria
  • Asthma group: Doctor's diagnosed asthma
  • Cystic Fibrosis group: A diagnosis of cystic fibrosis, confirmed by a sweat test or genetic analysis
  • Exclusion criteria
  • Recent course of prednisone or antibiotics (\< 1 month before test)
  • Passive smoking
  • Other chronic inflammatory disease (e.g. inflammatory bowel disease, rheumatic disease, auto-immune disease)
  • Healthy children:
  • No current or history of respiratory symptoms

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Number of participants with adverse events directly related to the various point-of-care tests used

Time Frame: Questionnaire will be done directly after specific test (1 day). No long term (S)AE is expected and measurement of each test is only performed once.

Any adverse event of any kind will be noted. Furthermore, each participant will be asked whether the test was easy to perform. This question can be answered on a 5-point scale (0=totally agree that test was easy to perform, 4= totally disagree that test was easy to perform)

Secondary Outcomes

  • Sensitivity and Specificity of new point-of-care Aeonose eNose in diagnosing asthma.(Measurements will be analysed within 6 to 12 months)
  • Sensitivity and Specificity of Ion Mobility Spectrometry in diagnosing asthma.(Measurements will be analysed within 6 to 12 months)
  • Sensitivity and Specificity of new point-of-care Aeonose eNose in diagnosing cystic fibrosis.(Measurements will be analysed within 6 to 12 months)
  • Sensitivity and Specificity of Ion Mobility Spectrometry in diagnosing cystic fibrosis.(Measurements will be analysed within 6 to 12 months)

Study Sites (1)

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