Comparison of the effects of epidural injection for labor analgesia: A randomized controlled trial
- Conditions
- Pregnancy, childbirth and the puerperium
- Registration Number
- KCT0004389
- Lead Sponsor
- Samsung Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 93
Among parturients who are scheduled to vaginal delivery
-American Society of Anesthesiologists class I. II
-primipara
-gestational age = 36 weeks
-Single child
-Cervical dilation = 5cm
-American Anesthesiologist Society class = III
-Long-term opioids user
-Patients injected intravenous opioid within 4 hours prior to labor analgesia
-Patients allergic to local anesthetics
-gestational age < 36 weeks
-multiple gestation
-multipara
-Preeclampsia
-Preterm Premature Rupture of Membranes
-non cephalic presentation
-Patients who are not suitable for nerve block as blood coagulation disorder
-Patients with advanced liver disease and severe renal impairment
-Patients with central nervous system disease
-Cardiac disease patients
-Patients taking drugs that are not suitable for anticoagulants and local anesthesia
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method to compare the difference in epidural analgesic consumptions used per hour to delivery among three groups
- Secondary Outcome Measures
Name Time Method the difference in the amount of epidural analgesia used per hour after delivery after vaginal delivery between the manual group and Programmed intermittent epidural bolus groups.;compare the differences in the request to delivery patient conrolled epidyral analgesia ratio;compare the difference in the degree of motor nerve block between manual group and programmed intermittent epidural bolus group