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Patellofemoral Pain After Unicondylar Knee Arthroplasty

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01407042
Enrollment
24
Registered
2011-08-01
Start date
2011-09-30
Completion date
Unknown
Last updated
2016-07-19

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

Conditions

Mobile-bearing Unicondylar Knee Arthroplasty

Keywords

unicondylar knee arthroplasty, mobile-bearing, patellofemoral pain

Brief summary

Unicondylar knee arthroplasty (UKA) is a proven procedure in patients suffering from unicompartmental knee osteoarthritis. Two different types of UKA design are available - both with different pros and cons. The so-called 'mobile-bearing UKA' requires the removal of an additional amount of cartilage and bone close to the implantat. It is unclear whether this is of clinical relevance. We speculate that the amount of cartilage/bone removal is related to the clinical outcome of the UKA-surgery. In patients receiving a mobile-bearing UKA that amount of cartilage/bone removal is measured during the surgery. The clinical success of the procedure will be determined with certain knee questionnaires (Kujala & KOOS)preoperatively, 3 months postoperatively, 6 months postoperatively and 1 year postoperatively. Additionally, the so-called bone-remodelling around that area of resected cartilage and bone will be measured (SPECT-CT) postoperatively. The three variables (removed amount of cartilage/bone; clinical success with regard to the questionnaires; bone remodelling) are then analyzed with statistical methods to find out potential assoziations among them.

Interventions

PROCEDUREmobile-bearing unicondylar knee arthroplasty

mobile-bearing unicondylar knee arthroplasty

Sponsors

Medical University Innsbruck
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

\- osteoarthritis or osteonecrosis in the medial or lateral tibiofemoral compartment

Exclusion criteria

* failed upper tibial osteotomy * insufficiency of the collateral or anterior cruciate ligaments * a fixed varus or valgus deformity (not passively correctable) above 15° * a flexion deformity greater than 15° * rheumatoid arthritis

Design outcomes

Primary

MeasureTime frameDescription
Size of anterior femoral notchday 0Required cartilage / bone removal adjacent to the femoral implant
Kujala Score changes-1 days, 3 months, 6 months, 1 year
KOOS questionnaire changes-1 days, 3 months, 6 months, 1 year
Radionuclide tracer uptake at the surgically created notch6 months

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026