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Continuous Regional Analgesia After Total Knee Arthroplasty

NCT00337597 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2008-07-21

No results posted yet for this study

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.

Conditions

  • Analgesia

Interventions

OTHER

Glucose 5%

OTHER

NaCl 0.9%

Sponsors & Collaborators

  • Nantes University Hospital

    lead OTHER

Principal Investigators

  • Charles Pham Dang, MD · Nantes UH

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-05-31
Primary Completion
2007-07-31
Completion
2007-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00337597 on ClinicalTrials.gov