Cesarean Section Clinical Trial
Official title:
A Comparison of Different Concentration Ropivacaine Combination With Fentanyl for Patient-controlled Epidural Analgesia After Cesarean Delivery
To compare the postoperative analgesic effect and the intensity of motor block in different concentration ropivacaine plus fentanyl when used epidurally with a patient-controlled analgesia device after Cesarean delivery.
1. Written informed consent must be obtained before any study specific procedures are
undertaken.
2. All patients were received epidural anesthesia with 2% Lidocaine and patient-controlled
epidural analgesia (PCEA) for post- operative pain control. PCEA randomly allocated
into three groups. Group A patients received 0.08% ropivacaine plus 4 mcg /mL fentanyl,
Group B patients received 0.08% ropivacaine plus 2mcg /mL fentanyl, and Group C
patients received 0.16 % ropivacaine plus 2 mcg /mL fentanyl. Dermographic data, dosage
of PCEA during first 48 hours post-operation,NRS scores, patient satisfaction and the
intensity of motor block will be recorded and analyzed.
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