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Lateral Retinacular Release in Total Knee Arthroplasty With Patellar Replacement

Systematic Lateral Retinacular Release Does Not Reduce Post-Operative Anterior Knee Pain After Primary Total Knee Arthroplasty With Patellar Replacement

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05778539
Enrollment
220
Registered
2023-03-21
Start date
2019-10-01
Completion date
2022-04-30
Last updated
2023-03-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anterior Knee Pain Syndrome

Keywords

Total knee arthroplasty, Patellar resurfacing, Lateral retinacular release, Anterior knee pain

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.

Interventions

PROCEDURELateral retinacular release

During the implantation of a total knee arthroplasty a lateral retinacular release is performed in the intervention group

Sponsors

Hospital del Mar
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
40 Years to 90 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline in Anterior Knee Pain at one year after surgeryAt the preoperative visit and at the 1-year follow upPressure 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 upThe 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

MeasureTime frameDescription
Change from baseline in patellar pain and function at one year after surgeryAt the preoperative visit and at the 1-year follow upPatellofemoral 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 upThe Knee Society Score, being 0 the worst and 100 the best possible result

Other

MeasureTime frameDescription
Change from baseline in Patelar Height at one year after surgeryAt the preoperative visit and at the 1-year follow upMeasured in the lateral radiographic view using the Caton-Deschamps index
Change from baseline in Patellar Tilt at one year after surgeryAt the preoperative visit and at the 1-year follow upMeasured in the axial radiographic view, as the angle subtended by the anterior intercondylar line and the equatorial line of the patella preoperatively or a line drawn through the prosthesis-bone interface postoperatively

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026