Comparison of Quadriceps-sparing Minimally Invasive and Medial Parapatellar Total Knee Arthroplasty

National Taiwan University

Status and phase: Completed; Phase 4

Conditions: Osteoarthritis

Treatments: Procedure: total knee arthroplastyinstruments

Study type: Interventional

Funder types: Other

Identifiers

NCT01160835

9561705022

Details and patient eligibility

About

Quadriceps-sparing minimally invasive total knee arthroplasty (TKA) with side-cutting instruments has been proposed to limit surgical dissection without compromising the surgical outcome. We conducted a prospective, randomized study to compare the outcomes of quadriceps-sparing TKA with conventional medial parapatellar TKA, with two-year follow-up.

We hypothesize that the quadriceps-sparing arthrotomy would not outperform the conventional medial parapatellar arthrotomy in TKA, in terms of postoperative recovery of quadriceps muscle strength, alignment of the prosthetic knee, and clinical outcome.

Full description

Eighty primary TKAs in sixty patients of osteoarthritis constituted this study. Patients were randomly assigned to either quadriceps-sparing (QS, 40 knees) or medial parapatellar (MP, 40 knees) group. All surgeries were designed to set the prosthesis with thefemoral component alignment of 7º valgus and the tibial component alignment perpendicular to tibial shaft. Outcome variables included knee function defined by Hospital for Special Surgery knee score, quadriceps muscle strength measured by isokinetic dynamometer, pain indicated on visual analogue scale, range of motion, and post-operative alignment measured on plain radiograph.

Enrollment: 80 patients

Sex: All

Ages: 30 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• advanced osteoarthritis with radiograph-evident narrowing of joint gap,
• with persistent symptoms after conservative treatment for at least 6 months, and
• patients' intention to receive the prosthetic TKA.

Exclusion criteria

• the knees with excessive deformity of femorotibial angle exceeding 15° varus or 10° valgus,
• flexion contracture exceeding 15°,
• active infection involving the knees, or
• knees received previous surgery.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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80 participants in 2 patient groups

Quadriceps-sparing total knee arthroplasty

Experimental group

Description:

Quadriceps-sparing arthrotomy with side-cutting instruments

Treatment:

Procedure: total knee arthroplastyinstruments

Medial parapatellar total knee arthroplasty

Active Comparator group

Description:

Medial parapatellar arthrotomy with front-cutting instruments

Treatment:

Procedure: total knee arthroplastyinstruments