None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 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
Exclusion criteria
Exclusion criteria: -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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| to compare the difference in epidural analgesic consumptions used per hour to delivery among three groups | — |
Secondary
| Measure | Time frame |
|---|---|
| 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 | — |
Countries
Korea, Republic of
Contacts
Samsung Medical Center