Continuous Regional Analgesia After Total Knee Arthroplasty

Status Completed

Clinical Trial Summary

This prospective, comparative and double blind study is aimed to determine if normal saline or dextrose 5% in water will modify the stimulation during the insertion of the stimulating catheter used for continuous femoral and sciatic blocks in total knee replacement.

Clinical Trial Description

The operator is blinded to the medium fluid to expand the perineural femoral and sciatic nerves before threading in the stimulating catheter. He records all the electric data of electrolocation of nerve, which will be compared to determine whether or not a difference in intensity is found between normal saline or dextrose 5% in water. ;

Study Design

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

Related Conditions & MeSH terms

Analgesia

Clinical Trial Details

NCT number	NCT00337597
Study type	Interventional
Source	Nantes University Hospital
Contact
Status	Completed
Phase	Phase 3
Start date	May 2006
Completion date	December 2007

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