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Reducing high respiratory drive to facilitate supported ventilation in ARDS patients: a pilot study

Reducing high respiratory drive to facilitate supported ventilation in ARDS patients: a pilot study - Supported ventilation in ARDS patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON38185
Enrollment
12
Registered
2013-12-20
Start date
2014-03-07
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

Acute respiratory distress syndrome severe lung syndrome

Interventions

Low dose rocuronium will be administered to decrease respiratory drive until the patient ventilates with a tidal volume ~6 ml/kg. This will be done in steps of 5 mg boluses. Ventilator modes will be

Sponsors

Universitair Medisch Centrum Sint Radboud
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: • age > 18 year • informed consent • ARDS according to the Berlin definition • RASS -4/-5 • tidal volume > 8 ml/kg during supported ventilation • esophageal EMG catheter with balloons in situ

Exclusion criteria

Exclusion criteria: • recent use of muscle relaxants / neuromuscular blocking agents (

Design outcomes

Primary

MeasureTime frame
The main study parameter is the ability to titrate rocuronium in order to decrease the tidal volume (Vt) to approximately 6 ml/kg (yes/no).

Secondary

MeasureTime frame
• Respiratory rate • Diaphragm activity (Edi) • Transpulmonary pressure • Transdiaphragmatic pressure • Work of breathing • Dynamic and static respiratory compliance • Neuroventilatory efficiency (tidal volume/Edi) • Neuromechanical efficiency (transdiaphragmatic pressure/Edi) • Patient-ventilator contribution to breathing: PVBC = (tidal volume/Edi, no-assist) / (tidal volume/Edi, assist) • Oxygenation index (arterial oxygen tension / fraction of inspired oxygen) • Patient-ventilator asynchrony

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)