NCT00910013
Completed
Phase 1
A Randomized Trial Comparing the Efficacy on Post-operative Analgesia of Intra-articular Ropivacaine Added to a Femoral Block After Total Knee Replacement
Hopital de l'Enfant-Jesus1 site in 1 country80 target enrollmentApril 2006
Overview
- Phase
- Phase 1
- Intervention
- Ropivacaine
- Conditions
- Total Knee Replacement
- Sponsor
- Hopital de l'Enfant-Jesus
- Enrollment
- 80
- Locations
- 1
- Primary Endpoint
- Narcotic consumption per 24 hours after surgery (mg/kg)
- Status
- Completed
- Last Updated
- 15 years ago
Overview
Brief Summary
Total knee replacement is a painful procedure. Many solutions have been proposed to diminish the post-operative doses of narcotics, including nerve blocks.
The purpose of the study is to compare if the adjunction of intra-articular ropivacaine to a femoral block is more effective on narcotics consumption than the block alone after TKR.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Primary total knee replacement
- •Age \> 18 years old
- •Accept the study
Exclusion Criteria
- •Revision surgery
- •Use of anticoagulants drugs
- •Neurologic disorder
- •Unable to sign consent form
Arms & Interventions
Ropivacaine + femoral block
After the surgery is proceeded and after the closure of the joint capsule, 20 cc of ropivacaine 0.5% is inserted intra-articular through a catheter.
Intervention: Ropivacaine
Outcomes
Primary Outcomes
Narcotic consumption per 24 hours after surgery (mg/kg)
Time Frame: 48 hours
Secondary Outcomes
- VAS score at 24 hours(48 hours)
Study Sites (1)
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