Prospective, bicentric observational study to assess a novel system for automated control of mechanical ventilation (Smart Vent Control, SVC) during general anesthesia.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Planned elective surgery of the upper limb, lower limb or peripheral vascular surgery in general anesthesia
* Patient is classified as American Society of Anesthesiologists physical status (ASA) I, II or III
* Age ≥ 18 years
* Written consent of the patient for study participation
Exclusion Criteria:
* Mild, moderate or severe acute respiratory distress syndrome (ARDS)\[10\]
* Known chronic obstructive pulmonary disease Gold stage III or higher
* Two or more of the following organ failures
* Mild, moderate or severe ARDS
* Hemodynamic instability: systolic blood pressure \< 90 mm Hg, mean arterial pressure \< 70 mm Hg or administration of any vasoactive drugs.
* Acute renal failure: oliguria (urine output \< 0.5 ml/kg/h for at least 2 hours despite of adequate management or creatinine increase \> 0.5 mg/dl
* Cerebral failure: loose of consciousness or encephalopathy
* Patient is pregnant.
What they're measuring
1
Frequency of adverse events.
Timeframe: During artificial ventilation with SVC (up to 8 hours).