Continuous Regional Analgesia After Total Knee Arthroplasty
NCT ID: NCT00337597
Last Updated: 2008-07-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE3
50 participants
INTERVENTIONAL
2006-05-31
2007-12-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Interventions
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Glucose 5%
NaCl 0.9%
Eligibility Criteria
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Inclusion Criteria
* 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
18 Years
90 Years
ALL
No
Sponsors
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Nantes University Hospital
OTHER
Responsible Party
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Nantes University Hospital
Principal Investigators
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Charles Pham Dang, MD
Role: PRINCIPAL_INVESTIGATOR
Nantes UH
Locations
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Departemental Hospital of la Roche sur Yon
La Roche-sur-Yon, , France
Nantes University Hospital
Nantes, , France
Countries
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Other Identifiers
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BRD 05/7-F
Identifier Type: -
Identifier Source: org_study_id