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NCT04461821Recruiting

Exhaled Breath Analysis by Secondary Electrospray Ionization - Mass Spectrometry in Children and Adolescents

Exhaled Breath Analysis by Secondary Electrospray Ionization - Mass Spectrometry in Children and Adolescents (EBECA)

Source: ClinicalTrials.gov · Last updated 8 May 2026

Brief summary (registry, in English)

This study is to investigate breath analysis (breath metabolomics) combined with established bioinformatic tools as a platform for companion diagnostics.

Status (registry)
Recruiting
Study type
Observational
Enrollment
3600 (estimated)
First submitted
23 Jun 2020
Start date
11 Sept 2020
Primary completion date
Jul 2030
Lead sponsor
University Children's Hospital Basel
NCT number
NCT04461821

What you commit to

  • Study type: Observational
  • Planned participants: 3600
  • From 11 Sept 2020 to the primary completion date, Jul 2030
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Physical or intellectual impairment precluding protocol adherence.
    • Additional exclusion criteria for respiratory disease population:
  • Known malignancy, active smoker (passive smoke exposure is not an exclusion criterium), known inflammatory diseases (e.g. autoimmune disease) that require medical and/or pharmacological treatment and is associated with an inflammatory response, relevant congenital defects
    • Additional exclusion criteria for neurological disease population:
  • Known malignancy, active smoker (passive smoke exposure is not an exclusion criterium), known inflammatory diseases (e.g. autoimmune disease) that require medical and/or pharmacological treatment and is associated with an inflammatory response, relevant congenital defects.
    • Additional exclusion criteria for T1D population:
  • Known malignancy, active smoker (passive smoke exposure is not an exclusion criterium), relevant congenital defects.

Who the study is looking for

  • Age 0 ≤ 22 years at study entry and signed informed consent
    • Additional inclusion criteria for respiratory disease population:
  • Acute disease: - Acute signs for a respiratory disease, indicated by e.g. increased work of breathing (e.g. dyspnea, increased respiratory rate), cough or wheezing.
  • Chronic disease: - Suspected or confirmed chronic airway disease (e.g. asthma).
    • Additional inclusion criteria for neurological disease population:
  • Acute disease: - Acute presentation or report within 24 hours of any signs of neurological deficit (motor function, sensoneural, or verbal).
  • Chronic disease: - Confirmed chronic neurologic disease (e.g. childhood epilepsy).
    • Additional inclusion criteria for T1D disease population:
  • Acute disease: - Hyperglycemia and/or pH (venous) \<7.3, bicarbonate \>10 mmol/L, increased levels of acetone in blood or urine in the context of newly diagnosed or known T1D.
  • Chronic disease: - Confirmed diagnosis of T1D

Age in the registry: - to 22 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Children's Hospital Basel (UKBB)
Coordinator of this site? Confirm its status
BaselSwitzerlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.