Investigation of lung ventilation during intensive care treatments measured by electrical impedance tomography in mechanically ventilated patients.

Investigation of lung ventilation during intensive care treatments measured by electrical impedance tomography in mechanically ventilated patients. - LUventEIT

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

DRKS

Registry ID

DRKS00010832

Enrollment

Registered

2016-07-19

Start date

2016-08-01

Completion date

Unknown

Last updated

2025-04-07

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

Conditions

Observational study: ventilated patients are monitored by EIT during 24 hours

Interventions

Group 1: Observational study: ventilated patients are monitored by EIT during 24 hours and the functional lung size is calculated breathwise.

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Indication for ventilation >24h

Exclusion criteria

Exclusion criteria: Patient that are ventilated less then 24h. Patient where EIT cannot be used.

Design outcomes

Primary

Measure	Time frame
WHAT: Functional lung size (FLS) by EIT, P/F-Ratio, CL (lung compliance), PaCO2 (partial pressure of carbon dioxide in arterial blood) WHEN: during 24h HOW: by EIT (electrical impedance tomography)	—

Secondary

Measure	Time frame
WHAT: Dependent SilentSpaces DSS, Non-dependent SilentSpaces NSS, Centre of Ventilation CoV, ventral ventilation in %, dorsal ventilation in %, right lung ventilation in %, left lung ventilation in % WHEN: during 24 hours, HOW: by EIT	—

Countries

Germany

Contacts

Public ContactJens Kraßler

Fachkrankenhaus Coswig GmbHAbteilung Anästhesiologie/Intensivtherapie

krasslerj@fachkrankenhaus-coswig.de03523/65-102

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026