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Clinical Trials/ACTRN12622001235796
ACTRN12622001235796
Not yet recruiting
未知

A pragmatic, randomized, multi-centre trial of protective versus conventional ventilation on the incidence of acute respiratory failure in adults patients undergoing major laparoscopic surgery

Austin Health0 sites1,750 target enrollmentSeptember 13, 2022

Overview

Phase
未知
Intervention
Not specified
Conditions
Post-operative pulmonary complications
Sponsor
Austin Health
Enrollment
1750
Status
Not yet recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
September 13, 2022
End Date
TBD
Last Updated
3 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Equal to or greater than 40 years
  • Scheduled to have major laparoscopic surgery (including robotic surgery) with an expected duration of more than two hours
  • Expected to have invasive arterial pressure monitoring as part of their routine care

Exclusion Criteria

  • Scheduled to have cardiac, thoracic, or intracranial neurological surgery
  • Need of nitrous oxide administration
  • Previously had lung surgery
  • Planned reintubation after surgery (e.g., planned re\-operations)
  • Received invasive ventilation for longer than 12 hours within the last 30 days prior to surgery
  • Any other contra\-indication to hypercapnia
  • Previous randomization into this clinical trial

Outcomes

Primary Outcomes

Not specified

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