RecruitingNCT04157361

Pulmonary Condensate: Non-invasive Evaluation of Pulmonary Involvement in Asthma and Cystic Fibrosis.

Pulmonary Condensate: A Promising Source of Proteomic Biomarkers for Non-invasive Evaluation of Pulmonary Involvement in Asthma and Cystic Fibrosis.


Sponsor

The Institute of Molecular and Translational Medicine, Czech Republic

Enrollment

450 participants

Start Date

May 1, 2015

Study Type

OBSERVATIONAL

Conditions

Summary

Exhaled breath condensate (EBC) represents a rich source for countless biomarkers that can provide valuable information about respiratory as well as systemic diseases. Finding non-invasive methods for early detection of lung injury, inflammation and infectious complications in chronic diseases like (CF) Cystic fibrosis or (AB) Bronchial asthma would be highly beneficial. Investigators propose to establish EBC "breathprints" revealing molecular signatures of pulmonary inflammation and specific respiratory bacterial infections of CF patients and AB. Investigators hypothesize that the analysis of EBC can reveal biomarkers specific for severity of the inflammation, and infection caused by opportunistic pathogens such as P. aeruginosa (PA). With these breath-prints, investigators also propose to establish correlations between respiratory microbiota using traditional methods and CF lung disease severity. Together, the studies will advance the development and validation of EBC as a novel tool for the proper diagnosis of AB and monitoring of CF disease activity, treatment efficacy and PA or another opportunistic infections.


Eligibility

Inclusion Criteria3

  • Children/adults with moderate or IgE mediated asthma
  • Children/adults with cystic fibrosis
  • Healthy control children/adults without lung disorders

Exclusion Criteria1

  • \-

Interventions

DIAGNOSTIC_TESTCollection of breath condensate

Breath condensate will be collected from the patients involved in study.


Locations(1)

University Hospital Olomouc

Olomouc, Czechia

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NCT04157361


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