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Clinical Trials/KCT0008379
KCT0008379
Recruiting
未知

sefulness of oxygen reserve index (ORI) to avoid excessive hyperoxia undergoing orthopedic or general trauma surgery during general anesthesia: A prospective, randomized, open study

Ajou University Hospital0 sites54 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Ajou University Hospital
Enrollment
54
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Ajou University Hospital

Eligibility Criteria

Inclusion Criteria

  • Trauma patients undergoing orthopedic or trauma surgery under general anesthesia
  • Patients with ASA class 3 or higher
  • Patients who have already had invasive arterial line or are scheduled to be placed and monitored during surgery
  • Age: 20 to 79 years old
  • Multiple trauma with/without heart or lung contusion
  • Patients undergoing induction of general anesthesia in the operating room or already intubated in a trauma bay or ICU
  • Patients with sufficient lung function to tolerate an initial FiO2 of up to 0\.5 immediately after intubation
  • Acute Respiratory Distress Syndrome ARDS, depending on the severity of ARDS, patients who can maintain SpO2 above 95% with an initial FiO2 of 0\.5
  • If the consent of the principal or a guardian in a legal representative relationship (when the consent of the individual is impossible due to intubation, etc.) can be obtained in advance

Exclusion Criteria

  • Patients unable to maintain an SpO2 of 95 or higher from an initial FiO2 of 0\.5 immediately after intubation

Outcomes

Primary Outcomes

Not specified

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