Combined Implementation of Dural Puncture Epidural and Programmed Intermittent Epidural Bolus for Labor Analgesia
Labor Pain, Labor Analgesia
About this trial
This is an interventional treatment trial for Labor Pain focused on measuring labor analgesia, dural puncture epidural (DPE), standard Epidural (EPL), continuous epidural infusion (CEI), programmed intermittent epidural bolus (PIEB)
Eligibility Criteria
Inclusion Criteria:
- women requeste labor analgesia
- ASA I or II
- at 37-42 weeks' gestation
- nulliparous
- singleton pregnancy, vertex presentation
- visual Numerical Rating Scale (VNRS) at requesting analgesia > 5 (NRPS 0-10)
- cervical dilatation < 5 cm
Exclusion Criteria:
- patient refusal to participate in the study
- age <20 years or >40 years
- body mass Index(BMI)>50 (Kg/m2)
- clinically significant diseases of pregnancy (i.e.,gestational hypertension, preeclampsia, gestational placenta previa, placental abruption diabetes)
- contraindications to neuraxial analgesia
- drug abuse
- conditions associated with an increased risk of a cesarean delivery (i.e., history of uterine anomaly or surgery, morbid obesity) and known anomalies
Sites / Locations
- Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Active Comparator
EPL and CEI
DPE and CEI
DPE and PIEB
Those with receive a standard epidural (EPL) and continuous epidural infusion(CEI) + patient-controlled epidural analgesia (PCEA)
Those with receive a dural puncture labor epidural (DPE) and continuous epidural infusion(CEI) + patient-controlled epidural analgesia (PCEA)
Those with receive a dural puncture labor epidural (DPE) and programmed intermittent epidural boluses(PIEB) + patient-controlled epidural analgesia (PCEA)