Status:
COMPLETED
Lidocaine Patches After Cesarean Section
Lead Sponsor:
Yale University
Conditions:
Postoperative Pain
Obstetric Pain
Eligibility:
FEMALE
18-52 years
Phase:
PHASE3
Brief Summary
The aim of this study is to investigate the impact of using lidocaine patches after cesarean section on pain control and opioid use in the immediate post-operative period. The hypothesis is the use of...
Detailed Description
The use of lidocaine as a local anesthetic is a common and widely used in practice. Lidocaine patches can be used for localized pain control and can be placed every 24 hours. The use of lidocaine patc...
Eligibility Criteria
Inclusion
- Female
- Primary or secondary cesarean delivery
- Able to consent to research study
Exclusion
- 3 or more prior cesarean deliveries
- History of abdominoplasty
- History of abdominal hernia repair with mesh
- Allergy to lidocaine
- Allergy to adhesives in medical tape
- Women who received general anesthesia for their cesarean delivery
- Women with active substance abuse
- Women methadone or suboxone for a history of opiate abuse
Key Trial Info
Start Date :
October 10 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 31 2022
Estimated Enrollment :
93 Patients enrolled
Trial Details
Trial ID
NCT04443569
Start Date
October 10 2021
End Date
August 31 2022
Last Update
November 6 2024
Active Locations (1)
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1
Yale New Haven Hospital
New Haven, Connecticut, United States, 06512