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Clinical Trials/KCT0002642
KCT0002642Recruiting未知

The effect of emergence FIO2 on postoperative lung volume

Samsung Medical Center0 sites81 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Recruiting
Enrollment
81

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional Study

Eligibility Criteria

Ages
18(Year) to 80(Year) (—)
Sex
All

Inclusion Criteria

  • 18-80 aged, ASA I-III patients undergoing elective laparascopic abdominal surgery

Exclusion Criteria

  • 1) patients who can not be applied the sensors of EIT device
  • 2) any abnomality in diaphragmatic function
  • 3) patients with any pace maker
  • 4) hemodynamic instability during the perioperative period, who transferred to postoperative ICU
  • 5) A woman in pregnancy
  • 6) Obese patient with BMI over 30-
  • 7) any neuromuscular disease patient
  • 8) preoperative active or chronic lung disease (chronic obstructive pulmonary disease, pneumonia, asthma)
  • 9) predicted airway difficulty
  • 10) patient who refuse to enroll to the study
  • 11) emergency operation

Investigators

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