Local Lidocaine Infiltration for Pain Management Post Cesarean Delivery.

• Status: Unknown status
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: Female

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.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Soroka University Medical Center
• Treatments: Lidocaine

Criteria

Inclusion Criteria:

• Women who are scheduled for an elective cesarean delivery under general/spinal analgesia using a transverse lower abdominal incision.

Exclusion Criteria:

• More than two previous cesarean deliveries

• Other abdominal operations in the past

• Morbid obesity

• Diabetes mellitus, neurological diseases, systemic vascular disease.

• Mental disability

• Lidocaine sensitivity