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Automated Minimization of Ventilator Energy to Improve Lung-Protective Ventilation

Automated Minimization of Ventilator Energy to Improve Lung-Protective Ventilation - AUPROVENT

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
DRKS
Registry ID
DRKS00013540
Enrollment
20
Registered
2017-12-01
Start date
2017-12-11
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

Invasive mechanical ventilation

Interventions

Group 1: Ventilation with "Adaptive Ventilation Mode" (AVM) for 1 hour Group 2: Ventilation with "Adaptive Ventilation Mode 2" (AVM2) for 1 hour

Sponsors

Universitätsklinikum Schleswig-Holstein
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Patients on invasive mechanical Ventilation on intensive care units - arterial line for invasive blood pressure measurement present - Age > 18 years - written informed consent

Exclusion criteria

Exclusion criteria: - expiratory time constant > 1.5 s - PaO2/FiO2 Ratio 70 mmHg despite optimization of Ventilator Settings by treating ICU physician - acute severe hemodynamic instability (mean arterial pressure 150/min OR heart rate < 40/min) - high frequency oscillatory Ventilation - spontaneous breathing activity

Design outcomes

Primary

MeasureTime frame
Tidal volume in ml per kg predicted body weight after one hour of mechanical ventilation with the respective mode (AVM or AVM2)

Secondary

MeasureTime frame
- Driving pressure (Difference between airway plateau pressure and end-expiratory airway pressure, cmH2O) - power of breathing (J/min) - arterial partial pressure of oxygen (mmHg) - arterial partial pressure of carbon dioxide (mmHg) - pH - alveolar Minute Ventilation (l/min, calculated as (tidal volume - Serial dead space volume) * respiratory rate) - mean airway pressure (cmH2O) - mean arterial pressure (mmHg) - heart rate (1/min, ECG)

Countries

Germany

Contacts

Public ContactTobias Becher

Universitätsklinikum Schleswig-Holstein Campus Kiel, Klinik für Anästhesiologie und Operative Intensivmedizin

tobias.becher@uksh.de+49 431 50020980

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 1, 2026