Menu
Recruiting NCT05456009

Exhaled Breath Analysis in Human Subjects

Observational Exhaled Breath Pattern After Medication Intake, in OSA Patients, or Other Pulmonary Diseases

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: No intervention.
Who it may be relevant to
Registry conditions: Exhaled Breath Pattern After Medication Intake, in OSA Patients, or Other Pulmonary Diseases. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Switzerland
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Exhaled Breath Analysis by Secondary Electrospray Ionization - Mass Spectrometry (SESI-MS) in Human Subjects

Overview

Identification of exhaled breath pattern of human subjects

Detailed description

Breath analysis with mass spectormetry as a non-invasive method to identfy exhaled breath patterns.

Interventions

  • Other No intervention
    No intervention

Primary outcome measures

  • Exhaled breath pattern [Time frame: baseline]
Secondary outcome measures (7)
  • Chemical structure of exhaled breath molecules [Time frame: baseline]
  • Body fluids [Time frame: baseline]
  • Disease marker [Time frame: baseline]
  • Distinguish between disease [Time frame: baseline]
  • Health state [Time frame: baseline]
  • Medication [Time frame: baseline]
  • Excretion of drugs [Time frame: baseline]

Eligibility criteria

Inclusion criteria

  • >= 18 years
  • Informed consent

Exclusion criteria

  • specific exclusion criteria for different subgroups

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Switzerland · 1 center
  • University Hospital Zurich — Zurich

Identifiers

NCT: NCT05456009 · 2019-00030

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗