About this trial
The purpose of this randomized controlled trial is to compare the efficacy and safety of two epidural analgesia maintenance methods for labor pain relief: Programmed Intermittent Epidural Bolus (PIEB) and Continuous Epidural Infusion (CEI), both combined with Patient-Controlled Epidural Analgesia (PCEA). The study aims to evaluate which technique provides superior analgesia while minimizing anesthetic consumption and preserving maternal motor function. A total of 60 parturients at Family Hospital, Da Nang, will be randomly assigned to either the PIEB or CEI group. Outcomes including pain intensity (VAS scores), total drug consumption, maternal satisfaction, and neonatal Apgar scores will be assessed.
Eligibility criteria
Qualifiers
Parturients indicated for labor analgesia for vaginal delivery via epidural anesthesia.
Age from 18 to 40 years.
Physical status: ASA II.
Singleton pregnancy, full-term, vertex presentation in labor.
Disqualifiers
Contraindications to epidural analgesia.
History of allergy to local anesthetics (Ropivacaine) or opioids (Fentanyl).
High-risk pregnancies: Preeclampsia, placenta previa, placental abruption.
Fetal distress or fetal abnormalities.
Trial design
Treatments tested in this trial
- PIEB + PCEA
- CEI + PCEA