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Lateral Retinacular Release in Total Knee Arthroplasty With Patellar Replacement

Not Applicable
Completed
Conditions
Anterior Knee Pain Syndrome
Interventions
Procedure: Lateral retinacular release
Registration Number
NCT05778539
Lead Sponsor
Hospital del Mar
Brief Summary

The aim of this study is to assess the effect of systematic lateral retinacular release on anterior knee pain, as well as its impact on the functional and radiological outcomes after total knee arthroplasty with patellar resurfacing.

Detailed Description

Anterior knee pain is an important cause of persistent pain after total knee arthroplasty. Lateral retinacular release has been proposed as a procedure to prevent anterior knee pain syndrome, based on the reduction of lateral tension and improving patellar tracking.

However, its effect on anterior knee pain after total knee arthroplasty is not clear when it is not strictly needed to correct maltracking.

The purpose of this trial is to evaluate the effect of systematic lateral retinaculare release on anterior knee pain, peformed during a total knee arthroplasty with patellar resurfacing.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
220
Inclusion Criteria
  • diagnosis of knee osteoarthritis
Exclusion Criteria
  • prior major surgery on the same knee (high tibial or distal femoral osteotomy, patellar realignment)
  • important preoperative malalignment (varus or valgus >15º or flexion deformity >15º)
  • inability to sign informed consent

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Lateral retinacular release groupLateral retinacular releaseDuring the implantation of a total knee arthroplasty a lateral retinacular release is performed
Primary Outcome Measures
NameTimeMethod
Change from baseline in Anterior Knee Pain at one year after surgeryAt the preoperative visit and at the 1-year follow up

Pressure pain threshold determined using pressure algometry

Change from baseline in Knee Pain measured by Visual Analogue Scale at one year after surgeryAt the preoperative visit and at the 1-year follow up

The Visual Analogue Scale referred by the patients at rest, when walking and when going up and downstairs. Scored between 0 (no pain at all) and 10 (maximum pain the patient could imagine).

Secondary Outcome Measures
NameTimeMethod
Change from baseline in patellar pain and function at one year after surgeryAt the preoperative visit and at the 1-year follow up

Patellofemoral score designed by Feller, distributed with a maximum of 15 points for the intensity of anterior knee pain, 5 points for quadriceps strength, 5 points for the ability to rise from a chair and 5 points for stair climbing ability

Change from baseline in knee fuction, measured by the Knee Society Score, at one year after surgeryAt the preoperative visit and at the 1-year follow up

The Knee Society Score, being 0 the worst and 100 the best possible result

Trial Locations

Locations (1)

Parc de Salut Mar

🇪🇸

Barcelona, Spain

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