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Unicondylar- or Total Knee Replacement? Patient Satisfaction, Function and Muscle Mass

Unicondylar - or Total Knee Replacement in Medial Gonarthritis? A Randomized Study of Patient Related Outcome Measures, Function and Muscle Mass

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02563756
Acronym
UKA or TKA?
Enrollment
80
Registered
2015-09-30
Start date
2015-09-30
Completion date
2025-09-30
Last updated
2020-10-26

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

Conditions

Knee Osteoarthritis

Keywords

Medial gonarthritis, knee osteoarthritis,, Muscle function, muscle mass, muscle atrophy, Total knee arthroplasty (TKA), Unicondylar knee arthroplasty (UKA), Total knee replacement (TKR), Unicondylar knee replacement (UKR), Health-related quality of life (HRQoL), Patient related outcome measurements (PROMs)

Brief summary

Patients with medial gonarthritis are randomised to a unicompartmental or a total knee replacement. Primary outcome: Thigh muscle cross sectional area and radiological attenuation measured by CT Secondary aims: functional tests, gait analysis, health related quality of life and patient related outcome.

Detailed description

Objective: The investigators aim with the present study was to compare patient related outcome measurements, knee function and muscle mass in patients operated with an UKR or a TKR for medial gonarthritis. Hypothesis: The investigators hypothesize that a greater number of patients might benefit from a less invasive surgery in terms of increased quality of life, function and muscle mass. Primary Outcome: Thigh muscle cross sectional area and radiological attenuation measured by CT. Secondary outcomes: Functional tests (timed up and go, 30s sit and stand, forward reach, forward step down, 6 min walk and 40 m walk test), knee strength (Biodex isokinetic dynamometer) and patient reported pain on a visual analogue scale (VAS). A number of PROMs: Health related quality of life (EQ-5D), Knee injury and Osteoarthritis Outcome Score (KOOS), Oxford Knee Score (OKS) and Forgotten Joint Score (FJS) as well as 3D movement and gait analysis. Inclusion criteria: Unilateral medial osteoarthritis of the knee (Kellgren 3b-4), aged 50 or above. Exclusion criteria: Insufficient anterior cruciate ligament (ACL). Fixed varus deformity \>10°, fixed flexion deformity \>10°, flexion \<100°. Previous high tibial osteotomy on the same side. Any neurological disease affecting strength or locomotion in any leg. Body mass index (BMI) \>35. Rheumatoid disease. Symptomatic osteoarthritis of the contra lateral knee or any hip. Insufficient written or spoken Swedish.

Interventions

Participants with a medial gonarthritis are operated with a medial unicompartmental prosthesis

PROCEDURETotal knee replacement

Participants with a medial gonarthritis are operated with a total knee replacement

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* medial gonarthritis, (Kellgren 3b-4) * correctible varus deformity less than 10 degrees * intact ACL * proficient in written and spoken swedish

Exclusion criteria

* Valgus gonarthritis * flexion deformity of 10 degrees * knee flexion of less than 100 degrees * previous high tibial osteotomy * neuromuscular disorders of lower extremities * symptomatic osteoarthritis of the contralateral knee or any hip.

Design outcomes

Primary

MeasureTime frameDescription
Muscle mass2 yearsThigh muscle cross sectional area and radiological attenuation measured by CT

Secondary

MeasureTime frameDescription
Muscle function2 yearsFunctional test of quadriceps strength, a stair negotiation test where the patient is asked to perform as many repetitions as possible in 30 seconds.
Health related outcome measurement, questionnaire2 yearsEQ5D, a qualitative measurement of patient perceived quality of life
Patient reported outcome measurement, knee function questionnaire (PROM).2 yearsKnee osteoarthritis outcome score (KOOS).

Countries

Sweden

Contacts

Primary ContactMargareta Hedström, MD, PhD
margareta.hedstrom@ki.se+4670735959
Backup ContactNicolas Martinez, MD
+46709900089

Outcome results

None listed

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