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Clinical Trials/KCT0006367
KCT0006367Recruiting未知

A comparison between total intravenous anesthesia (Propofol) and inhalational (Sevoflurane) in improving postdischarge nausea and vomiting

Soon Chun Hyang University Hospital Bucheon0 sites186 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Recruiting
Sponsor
Enrollment
186

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional Study

Eligibility Criteria

Ages
20?(Year) to 50?(Year) (—)
Sex
Female

Inclusion Criteria

  • Patients between the ages of 20 and 50 who are scheduled to be discharged on the same day after performing cervical conical resection in the hospital.

Exclusion Criteria

  • Postoperative opioid use
  • In case of hospitalization due to severe PONV

Investigators

Sponsor
Soon Chun Hyang University Hospital Bucheon

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