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Clinical Trials in Italy / NCT07646249
Recruiting Observational

VENtilation Modalities During Transport of PostoperatIve CRITically Ill Patients to the ICU

NCT07646249 · tracked via the Priya Life Science Italy tracker
Sponsor
Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva
Phase
Observational
Started
2026-09-07
Last updated
2026-09-11

Condition(s) studied

Respiration, ArtificialPositive-Pressure RespirationPostoperative Complications (Cardiopulmonary)Postoperative ComplicationsCritical IllnessIntensive Care Units

Study summary

Patients undergoing major non-cardiac surgery may require postoperative mechanical ventilation and transfer from the operating room to the intensive care unit (ICU). This intra-hospital transport phase is critical, as patients may experience changes in respiratory and hemodynamic status, including alterations in oxygenation, ventilation, blood pressure, and heart rate.

During transport, ventilatory support may be provided using different strategies, including manual ventilation with a bag-valve device or mechanical ventilation with a portable ventilator. Although both approaches are commonly used in clinical practice, there is limited evidence comparing their effects on respiratory function, gas exchange, and overall physiological stability during and after transport.

This multicenter, prospective observational study aims to describe current clinical practices in ventilatory support during intra-hospital transport in adult patients undergoing non-cardiac surgery who require ICU admission. The study will also evaluate changes in vital signs, arterial blood gas parameters, and respiratory mechanics, as well as the occurrence of adverse events during transport and postoperative pulmonary complications within the first five days after surgery.

No additional interventions or procedures beyond standard clinical care will be performed. All data will be collected as part of routine clinical practice. The results of this study are expected to improve the understanding of ventilation management during transport and to identify safer and more effective strategies for critically ill postoperative patients.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion criteria * Intubated patients undergoing general anesthesia for non-cardiac surgery * Requirement for postoperative IMV * Age ≥18 years * Obtained informed consent Exclusion criteria * Patients undergoing cardiac surgery * Patients receiving preoperative mechanical ventilation prior to surgery.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Azienda Ospedaliero-Universitaria di Alessandria Alessandria Italy Recruiting

More Societa Italiana Anestesia Analgesia Rianimazione e Terapia Intensiva trials in Italy

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07646249 on ClinicalTrials.gov ↗ ← All trials in Italy