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
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.
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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