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Clinical Trials/KCT0001391
KCT0001391Completed未知

A comparison of the anesthetic quality and side effects of epidural vs spinal anesthesia for emergency cesarean sections after labor epidural analgesia.

Cheil General Hospital & Women's healthcare center0 sites220 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
220

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

  • 1)By consent to participate in the study, those who signed the agreement in writing
  • 2)ASA(American society of Anesthesiology) scoring 1-2 patients scheduled for intrapartum cesarean section
  • 3)Parturient who epidurla analgesia

Exclusion Criteria

  • 1)The parturients more than ASA(American society of Anesthesiology) 3
  • 2)Contraindication to regional anesthesia
  • 3)Scheduled general anesthesia

Investigators

Sponsor
Cheil General Hospital & Women's healthcare center

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