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Clinical Study of Patellar Resurfacing and Non-resurfacing in Total Knee Arthroplasty

A Prospective Randomized Clinical Study of Patellar Resurfacing and Non-resurfacing in One-stage Bilateral Total Knee Arthroplasty

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03600922
Enrollment
66
Registered
2018-07-26
Start date
2011-03-31
Completion date
2017-08-31
Last updated
2018-07-27

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

Conditions

Total Knee Arthroplasty

Keywords

Osteoarthritis, Patellar resurfacing, Anterior knee pain

Brief summary

The literature regarding resurfacing of the patella in total knee arthroplasty has conflicting conclusions. This study assesses medium-term clinical results of total knee arthroplasties performed with and without the patellar resurfacing in patients undergoing single-staged bilateral total knee arthroplasty in a randomized controlled, clinical study at a minimum of 5 years follow-up.

Detailed description

Sixty-six patients (132 knees) underwent primary single-staged bilateral total knee arthroplasty for osteoarthritis. Patients were randomized to receive resurfacing or retention of the patella. All patients received the Scorpio NRG knee prosthesis. Evaluations were done preoperatively and yearly, up to a minimum of 5 years postoperatively. Knee Society Score and Feller Score outcomes were measured. Anterior knee pain, the clunk of patella, and patient satisfaction questionnaires were completed.

Interventions

PROCEDUREthe patella was resurfaced.

Patellar resurfacing was undertaken using a cemented, inset domed component in TKA.

Sponsors

Liaocheng People's Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* degenerative OA * 50-75 years * All patients with OA were bilateral knee OA

Exclusion criteria

* previous patellectomy * inflammatory arthritis * patellar fracture * patellar instability * previous extensor mechanism procedures * high tibial osteotomy, * severe valgus or varus deformity (\> 20°), severe flexion contracture (\> 30°) * previous unicondylar knee replacement * a history of septic arthritis or osteomyelitis.

Design outcomes

Primary

MeasureTime frameDescription
Change From Baseline in the Feller scoreBaseline,1,2,3,4 and 5 yearsThe Feller score consists four parts.Total score is 30 score (0-30) and the higher values represent a better outcome. The Feller score has points for Anterior knee pain (0 worst-15 best), quadriceps strength (1 worst -5 best) , ability to rise from chairand stability(0 worst-5 best )and stair-climbing(2 worst-5 best ). The scores from each item are summed to produce a total score
Change From Baseline in visual analogue scale (VAS)Baseline,1,2,3,4 and 5 yearsThe Visual analogue scale (VAS)is ranging from 0 to 10 points, with 0 being no pain and 10 being maximum pain.The higher values represent a worse outcome.
Change From Baseline in knee society score ( KSS)Baseline,1,2,3,4 and 5 yearsThe knee society score ( KSS) which consists of a 100-point scale for knee score and 100-point score for function score. The knee score has points for pain (0 worst -50 best ), range of motion (0 worst -25 best ) and stability (0 worst -25 best ). scores from each item are summed to produce a total score .The function score has points for walking ability (0 worst -50 best ) and stair climbing ability (0 worst -50 best ), scores from each item are summed to produce a total score.The knee score and the function score are recorded respectively.The higher values represent a better outcome.
Change From Baseline in anteroposterior long weight-bearing X-rayBaseline,1,2,3,4 and 5 yearsanteroposterior long weight-bearing X-ray
Change From Baseline in MOS item short from health survey(SF-36)Baseline,1,2,3,4 and 5 yearsThe MOS item short from health survey(SF-36) was constructed to survey health status in the Medical Outcomes Study. The SF-36 was designed for use in clinical practice and research, health policy evaluations, and general population surveys. The SF-36 includes one multi-item scale that assesses eight health concepts: 1) limitations in physical activities because of health problems; 2) limitations in social activities because of physical or emotional problems; 3) limitations in usual role activities because of physical health problems; 4) bodily pain; 5) general mental health (psychological distress and well-being); 6) limitations in usual role activities because of emotional problems; 7) vitality (energy and fatigue); and 8) general health perceptions.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026