Local Lidocaine Infiltration for Pain Management Post Cesarean Delivery.
Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
Participant gender:
Summary
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.