Status:
COMPLETED
Optimal Site of Administration for Continuous Wound Infusion After Cesarean Section
Lead Sponsor:
Association pour la Recherche et la Formation en Anesthésie Analgésie Réanimation
Conditions:
Cesarean Section
Eligibility:
FEMALE
18+ years
Phase:
PHASE3
Brief Summary
The purpose of this randomized double-blind study is to evaluate in which anatomical layer (AF versus BF) continuous wound infusion of local anesthetics combined with NSAIDs through a multiorifice cat...
Eligibility Criteria
Inclusion
- elective Cesarean Section under spinal anesthesia over37 weeks' gestation
Exclusion
- allergy to NSAIDs
- ASA III or higher
- refusal to participate
Key Trial Info
Start Date :
October 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2008
Estimated Enrollment :
56 Patients enrolled
Trial Details
Trial ID
NCT01160913
Start Date
October 1 2007
End Date
December 1 2008
Last Update
July 13 2010
Active Locations (1)
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1
Hôpital Cochin
Paris, France, 75014