Local Lidocaine Infiltration for Pain Management Post Cesarean Delivery.
NCT00737542 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL
Last updated 2009-11-26
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.
Conditions
- Pain
- Cesarean Delivery
Interventions
- DRUG
-
lidocaine
- DRUG
-
NACL 0.9%
Sponsors & Collaborators
-
Soroka University Medical Center
lead OTHER
Eligibility
- Min Age
- 18 Years
- Max Age
- 45 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
Countries
- Israel
Study Locations
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