Status:
TERMINATED
Comparison of Two Types of Pain Relief After Cesarean Delivery
Lead Sponsor:
Hopital Foch
Conditions:
Cesarean Section
Eligibility:
FEMALE
18-40 years
Phase:
PHASE4
Brief Summary
Women undergoing elective cesarean delivery, performed under a standard spinal anesthesia, will be randomized to undergo either TAP block or incisional infiltration with local anesthetic, in addition ...
Eligibility Criteria
Inclusion
- scheduled cesarean section performed under spinal anesthesia
- ASA I or II
- height above 1,55 m
- singleton pregnancy
Exclusion
- contre indication to a drug used in the study (levobupivacaine, ketoprofen, nefopam)
Key Trial Info
Start Date :
October 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2012
Estimated Enrollment :
77 Patients enrolled
Trial Details
Trial ID
NCT01151943
Start Date
October 1 2010
End Date
July 1 2012
Last Update
November 3 2016
Active Locations (1)
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1
Hôpital Foch
Suresnes, France, 92150