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BREathprint Variation during Intubation, mechanical ventilation and Anesthesia.

BREathprint Variation during Intubation, mechanical ventilation and Anesthesia.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24277
Enrollment
25
Registered
2011-02-11
Start date
2011-01-01
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

Ventilator associated lung injury

Interventions

None listed

Sponsors

Academic Medical Center, Amsterdam
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Planned elective surgery (with planned intubation >5h); 2. Informed consent; 3. Anesthesia with intravenous anesthestics.

Exclusion criteria

Exclusion criteria: 1. < 18 years of age; 2. History of any chronic or acute pulmonary condition (asthma, COPD, CF, pulmonary malignancy or acute lung injury); 3. Intubation and mechanical ventilation within the last 7 days.

Design outcomes

Primary

MeasureTime frame
1. Breathprint (exhaled biomarkers) as obtained by electronic nose measurement (Cyranose and ContiNose); 2. Systemic biological markers of oxidative stress and lung injury (e.g. Urin acid, IL-1b, IL-6, IL-8, TNFa en MPO).

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)