vaginal delivery
Conditions
Interventions
group A:2 ml of 0.125% bupivacaine plus 5 ug fentanyl for spinal anesthesia, 0.125% bupivacaine with 2 ug/mL fentanyl by PCEA
group B:2 ml of 0.125% ropivacaine plus 5 ug fentanyl for spinal anesthesia, 0.125% ropivacaine with 2 ug/mL fentanyl by PCEA
Sponsors
Changting Yan
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: This study included nulliparous parturients at greater than 37 weeks of gestation and with a cervical dilation of 3cm, ASA physical status I and II, request for labor analgesia, more than 18 year old, no sign for cesarean section, full-term pregnancy without any contraindications to neuraxial anesthesia.
Exclusion criteria
Exclusion criteria: Parturients were excluded if they were less than18 year-old, allergy to any study drugs or had Contraindications to neuraxial anesthesia and obstetric factors are not suitable for vaginal delivery, previous cesarean delivery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| MMT;Analgesic effect; | — |
Secondary
| Measure | Time frame |
|---|---|
| general condition;Non-invasive Blood Pressure;Heart Rate;labor condition;Apgar Score; | — |
Countries
China
Contacts
Public ContactChangting Yan
Liaocheng Dongchangfu District Health Center for Women & Children
Outcome results
None listed