About this trial
Patients receives induction of general anesthesia for interventional tricuspidal clipping and standard monitoring for this procedure including arterial and central venous line and transesophageal ultrasound. A cuirass for extrathoracal negative pressure ventilation is placed onto the chest but not switched on. During usual positive pressure ventilation a ventilatory, a hemodynamic and a 3D full volume ultrasounddataset of the right and left ventricle is recorded and severity of tricuspidal regurgitation examined. Afterwards negative pressure ventilation is started and positive pressure ventilation reduced as far as possible without reduction of tidal volumes. The same dataset of ventilation, hemodynamics and ultrasound is collected again during negative pressure ventilation. Afterwards the cuirass gets removed, study finished and everything proceeds as during standard procedure.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
patients planned for tricuspidal clipping
Disqualifiers
ventilatory of hemodynamic instability
fitting of cuirass not possible
unavailability of examiner
Trial population
All patients for tricuspidal clipping without an exclusion criterium
Trial design
Other
Other
Treatments tested in this trial
Negative Pressure Ventilation
DeviceSubstitution of positive pressure ventilation by negative pressure ventilation
Treatment groups
Trial outcomes
Primary outcomes
stroke volume index
transesophageal ultrasound measurement
Secondary outcomes
RVEF
transesophageal ultrasound measurement
LVEF
transesophageal ultrasound measurement
volumes of chambers
transesophageal ultrasound measurement
strain
transesophageal ultrasound measurement
Sponsors and contacts
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