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Clinical Trials/NCT01225484
NCT01225484
Unknown
Phase 4

Perioperative Analgetic Therapy After Knee Arthroplasty

Landeskrankenhaus Feldbach1 site in 1 country123 target enrollmentOctober 2010

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Knee Arthroplasty
Sponsor
Landeskrankenhaus Feldbach
Enrollment
123
Locations
1
Primary Endpoint
Static and dynamic pain scores (VAS)
Last Updated
11 years ago

Overview

Brief Summary

The purpose of this study is to compare two accepted methods of pain control in knee arthroplasty surgery.The first method combines the periarticular injection of ropivacaine with continuous blockade of the femoral nerve.The second method uses periarticular infiltration of ropivacaine in combination with an bolus of ropivacaine into an intraarticular catheter placed intraoperatively followed by a continuous intraarticular infusion of ropivacaine. All patient will also receive a sustained-release oral opioid and oral rescue opioids determined by pain severity using the Visual Analog Scale (VAS)

Registry
clinicaltrials.gov
Start Date
October 2010
End Date
October 2015
Last Updated
11 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Karl Trauner

M.D.

Landeskrankenhaus Feldbach

Eligibility Criteria

Inclusion Criteria

  • Elective primary knee arthroplasty
  • ASA I,II,\&III patients
  • Spinal Anaesthesia

Exclusion Criteria

  • Patients refusing consent
  • Contraindications to regional anaesthesia
  • Preexisting neurological disease
  • Alcohol or drug abuse
  • Inability to use the outcome assessment tools
  • Wheel chair or walker dependent
  • Pregnancy

Outcomes

Primary Outcomes

Static and dynamic pain scores (VAS)

Time Frame: 72 h

Secondary Outcomes

  • Maximum knee flexion (active/passive)>= 90°(72 h)

Study Sites (1)

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