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Clinical Trials/KCT0006917
KCT0006917
Completed
未知

Type of anesthesia in surgical conditions and postoperative recovery in laparoscopic surgery : a randomized trial comparing propofol-remifentanil total i.v. anesthesia with sevoflurane-remifentanil anesthesia.

Samsung Medical Center0 sites130 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
Samsung Medical Center
Enrollment
130
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
April 28, 2022
Last Updated
3 years ago
Study Type
Interventional Study
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Adult patients scheduled for elective laparoscopic colorectal cancer surgery (anterior resection, lower anterior resection, hemicolectomy) in which the main surgical procedure was expected to last for more than 1 hour were screened for eligibility.

Exclusion Criteria

  • \- Patients simultaneously participating in other studies
  • \- Patients scheduled to be transfered to the intensive care unit after surgery
  • \- Patients with a severe grade obstructive or restrictive pattern on PFT
  • \- High risk (expected postoperative event \> 5%) in cardiologic consultation
  • \- Patients with reduced renal function expected to delay recovery when using rocuronium due to severe renal impairment (Cr \> 1\.5mg/dL, eGFR \< 40 mL/min/1\.73m2\)
  • \- Patients with Obesity BMI\>40kg/m2
  • \- Patients with known allergies to medications or foods

Outcomes

Primary Outcomes

Not specified

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