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Patient Outcomes and Adverse Events in Mobile vs. Fixed Bearing Unicompartmental Knee Arthroplasty: A Randomized Controlled Trial

Comparison of post operative patient reported outcomes and adverse events in mobile bearing versus fixed bearing unicompartmental knee arthroplasty: Randomized Controlled Trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101136
Enrollment
60
Registered
2026-01-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: M170- Bilateral primary osteoarthritis of knee Health Condition 2: M171- Unilateral primary osteoarthritisof knee

Interventions

Intervention1: Mobile-bearing unicompartmental knee arthroplasty: Patients randomized to this group will undergo unicompartmental knee arthroplasty using a mobile-bearing tibial insert for isolated un

Sponsors

AIIMS Jodhpur
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Primary Medial UKA Antero medial compartment varus OA knee Flexion more than 90 degrees FFD less than 10 degrees Varus deformity less than 20 degrees

Exclusion criteria

Exclusion criteria: Graded 2 to 4 degenerative changes of lateral compartment history of lateral meniscectomy anterior cruciate ligament absence Revision surgery Previous lower limb surgery

Design outcomes

Primary

MeasureTime frame
Primary outcome of this study is to compare functional outcomes of the 2 groups using scores lik KSS, KFS, IKDC, WOMAC, KOOSTimepoint: 6 months—

Secondary

MeasureTime frame
Secondary outcome of this study is compare functional and clinical outcomes between 2 groups in the form of blood investigations and gait analysis etcTimepoint: 6 months—

Countries

India

Contacts

Public ContactRitvik Sharma

All India Institute Of Medical Sciences, Jodhpur

dr.saurabhortho@gmail.com7023578365

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026