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Optimal Site of Administration for Continuous Wound Infusion After Cesarean Section

Cesarean Section Clinical Trial

Official title:
Evaluation of Optimal Anatomical Layer for Continuous Wound Infusion of Local Anesthetics Combined With NSAIDs Through a Multiorifice Catheter for Postoperative Pain Intensity After Elective Cesarean Delivery

Clinical Trial 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 catheter has the best effectiveness during the first 48 hours on postoperative pain intensity after elective cesarean delivery.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01160913
Study type Interventional
Source Association pour la Recherche et la Formation en Anesthésie Analgésie Réanimation
Contact
Status Completed
Phase Phase 3
Start date October 2007
Completion date December 2008
View Details
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