Status:
COMPLETED
Continuous Regional Analgesia After Total Knee Arthroplasty
Lead Sponsor:
Nantes University Hospital
Conditions:
Analgesia
Eligibility:
All Genders
18-90 years
Phase:
PHASE3
Brief 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 fo...
Detailed 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 ner...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- American Society of Anesthesiologists (ASA) I and II
- Male or non-pregnant female
- 18 - 80 years of age
- Not allergic to iodine or local anesthetics
- Absence of abnormality of coagulation
- Scheduled for total knee replacement
Exclusion
Key Trial Info
Start Date :
May 1 2006
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2007
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00337597
Start Date
May 1 2006
End Date
December 1 2007
Last Update
July 21 2008
Active Locations (2)
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1
Departemental Hospital of la Roche sur Yon
La Roche-sur-Yon, France, 85000
2
Nantes University Hospital
Nantes, France, 44093