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Local Assessment of Ventilatory Management During General Anesthesia for Surgery

Local Assessment of Ventilatory Management During General Anesthesia for Surgery - a Prospective Observational Multi-center Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01601223
Acronym
LAS VEGAS
Enrollment
10690
Registered
2012-05-17
Start date
2013-01-31
Completion date
2013-11-30
Last updated
2015-10-14

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

Conditions

Anaesthesia, Lung Injury, Pneumonia, Pneumothorax, Respiratory Distress Syndrome, Adult, Respiratory Insufficiency, Surgery, Ventilator-Induced Lung Injury

Keywords

Ventilatory Management, Mechanical Ventilation, Post Operative pulmonary complications, Intra-operative complications, General Anesthesia, Surgery, LAS VEGAS, ESA (European Society of Anaesthesiology), European Society of Anaesthesiology

Brief summary

Objectives 1. To characterize mechanical ventilation practices during general anesthesia for surgery 2. To assess the dependence of intra-operative and post-operative pulmonary complications on intra-operative Mechanical Ventilation (MV) settings

Detailed description

Research questions * What MV-settings are used during general anesthesia for surgery? * Do MV-settings vary in and/or between centers? * Do MV-settings vary internationally? * Are MV-settings associated with incidence of intra-operative pulmonary complications? * Are MV-settings associated with incidence of post-operative pulmonary complications?

Interventions

None listed

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
CollaboratorOTHER
European Society of Anaesthesiology
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * All surgical procedures requiring invasive mechanical ventilation (MV)during general anesthesia for laparoscopic or non-laparoscopic surgery. * This includes MV performed with supra-glottic devices (e.g. laryngeal mask) * This includes patients receiving MV at the onset of the procedure (e.g. Intensive Care Unit patients) * This includes patients who will receive one-lung ventilation during the procedure

Exclusion criteria

* Obstetric surgical procedures or any procedure during pregnancy * Surgical procedures outside the operating room * Surgical procedures involving extra-corporal circulation

Design outcomes

Primary

MeasureTime frameDescription
Post-operative pulmonary complications, possibly related to ventilation strategyPost-operative on day of surgery, day 1, 2,3,4,5 and day 28Effect of Mechanical Ventilation settings during general anesthesia for surgery on the incidence of post-operative pulmonary complications (new or prolonged invasive or non-invasive mechanical ventilation, need for oxygen therapy, respiratory failure, pneumonia, ARDS 'Acute Respiratory Distress Syndrome', pneumothorax) Defined post-operative pulmonary complications are recorded from the medical chart on day 0, 1, 2, 3, 4 and 5 after surgery. On day 28 length of hospital stay and in hospital death are assessed.

Secondary

MeasureTime frameDescription
Intra-operative complications related to the ventilation strategyTime point(s) at which outcome measure is assessed is is: Day of surgery, day 1, 2, 3, 4, 5 and 28 after surgery
Mechanical ventilation-settings during general anesthesia for surgeryDuring the surgical procedure, from moment of to tracheal extubation or discharge from operation room (in case patient remains on mechanical ventilation)* Variation of applied MV settings within centers * Variation of applied MV settings between centers on an international basis

Countries

Estonia, Germany, Italy, Lithuania, Netherlands, Norway, Slovenia, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 9, 2026