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Exhaled breath analysis to diagnose acute lung injury.

Bedside exhaled breath octane measurements for the diagnosis and monitoring of acute respiratory distress syndrome in intubated and mechanically ventilated patients.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON27817
Enrollment
500
Registered
2018-07-19
Start date
2019-01-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ARDS, non-invasive diagnostic tests, early detection, octane Dutch: ARDS, niet-invasieve diagnostische methoden, vroege detectie, octane

Interventions

None listed

Sponsors

Amsterdam UMC, locatie AMC.
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Intubated and mechanically ventilated for less than 48 hours.

Exclusion criteria

Exclusion criteria: • Patient is expected to be deceased within 24 hours. • Exhaled breath collection deemed inappropriate by the attending physicians. • Active withdrawal from the study by the patient or his/her legal representative. • Present admission to the ICU is a readmission.

Design outcomes

Primary

MeasureTime frame
Exhaled breath concentration of octane, measure by compact gas-chromatography.

Secondary

MeasureTime frame
• Volatile organic compounds in exhaled breath measured by gas-chromatography and mass-spectrometry. • Protein patterns in fluid from the heat-moist exchanger. • Non-invasive imaging techniques: o Lung ultrasound o Electrical impedance tomography. • Lung injury prediction score. • ARDS as defined by the Berlin Definition • Therapeutic response in ARDS patients • ARDS phenotypes defined by clinical characteristics and by a biomarker profile of plasma biomarkers

Contacts

Public ContactLieuwe D.J. Bos

Academic Medical Center, Room G3-228 Meibergdreef 9

l.d.bos@amc.uva.nl+31 (0)20 5666345

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)