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Clinical Trials/NL-OMON36531
NL-OMON36531
Completed
N/A

Protective ventilation during general anesthesia for abdominal surgery * a randomized controlled trial - PROVHILO

Academisch Medisch Centrum0 sites100 target enrollmentTBD

Overview

Phase
N/A
Intervention
Not specified
Conditions
Ventilator associated lung injury
Sponsor
Academisch Medisch Centrum
Enrollment
100
Status
Completed
Last Updated
last year

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Planned elective abdominal surgery
  • \- General anesthesia with intravenous medication
  • \- High or intermediate risk for postoperative pulmonary complications (ARISCAT risk score \* 26\)

Exclusion Criteria

  • \- Age \< 18 years
  • \- Body mass index \> 40 kg/m2
  • \- Laparoscopic surgery
  • \- Previous lung surgery (any)
  • \- Persistent hemodynamic instability, intractable shock (considered hemodynamic unsuitable for the study by the patient\*s managing physician)
  • \- History of previous severe chronic obstructive pulmonary disease, COPD (non\*invasive ventilation and/or oxygen therapy at home or repeated systemic corticosteroid therapy for acute exacerbations of COPD)
  • \- Recent immunosuppressive medication (patients receiving chemotherapy or radiation therapy, within the last 2 months)
  • \- Severe cardiac disease (New York Heart Association class III or IV, or acute coronary syndrome, or persistent ventricular tachyarrhythmia\*s)
  • \- Mechanical ventilation \> than 30 minutes within last 30 days
  • (e.g., in cases of general anesthesia because of surgery)

Outcomes

Primary Outcomes

Not specified

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