MedPath

A randomized,double-blind, parallel-group multicenter study for the effect of an epidural top up with normal saline in combined spinal epidural anesthesia with isobaric bupivacaine for cesarean sectio

Not Applicable
Conditions
Patient for elective cesarean section,with analgesic level is below Th7 five minutes after the spinal anesthesia
Registration Number
JPRN-UMIN000014872
Lead Sponsor
Yokohama City University School of Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Female
Target Recruitment
80
Inclusion Criteria

Not provided

Exclusion Criteria

Emergency Gestational period <37 or >42 weeks Placenta previa Multiplets Severe PIH Bleeding disorders and coagulopathy Neuromuscular disease Spinal disorder with anatomical spinal anomaly A case of preliminary anesthetic treatment Body weight => 90kg Height < 150 and =>171 cm Major fetal anomaly Mental retardation Patient without cooperation History of allergy to local anesthetics

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time to reach Th4 on analgesic level(pin prick test),the percentage of patients that attain the analgesic level with Th4,attained maximum analgesic level
Secondary Outcome Measures
NameTimeMethod
Perioperative hemodynamics Total consumption of vasopressor agent Total consumption of intraoperative additional analgesic agent Intraoperative nausea and vomiting Volume of intraoperative urine, operation time, anesthesia time Apgar score Umbilical code blood gas analysis Post dural puncture headache and post-operative nausea and vomiting Total consumption of post-operative additional analgesics Post-operative VAS scale
© Copyright 2025. All Rights Reserved by MedPath