Pain Clinical Trial
Official title:
A Prospective Randomized Double-blind, Placebo-controlled Study of the Effect of Preoperative Analgesia With Local Lidocaine Infiltration for Pain Management Post Cesarean Delivery.
The objective of this prospective, double-blinded, placebo-controlled, randomized study is to evaluate the impact of preemptive analgesia using incisional site infiltration of lidocaine as compared to saline solution on post operative pain control in women undergoing cesarean deliveries.
The studied population would be based on women who are scheduled for an elective cesarean
delivery under general/spinal analgesia using a transverse lower abdominal incision.
Prior to each operation, the surgeon will be provided with a syringe containing a 20 mL
solution of 1% lidocaine or 0.9% sodium chloride, which will be injected subcutaneously to
the incisional site region after anesthesia and before the beginning of the surgery.
After the operation the conventional post cesarean analgesic regime will be used and recorded
for all women.
The self-report of pain will be assessed by the patient using a validated visual analog
scale, as instructed by the nursing staff.
The patient's mark will be used as a numerical index of pain intensity. The reports will be
taken by the patients in intervals of 4 hours for 48 hours after the operation. In addition,
analgesic requirements of the patient will be monitored and recorded by the nursing staff and
used for comparison between the two study group
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