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Study identifier: NCT06158646 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Mechanically or Kinematically Aligned Total Knee Prosthesis

Condition: Osteoarthritis, Knee  ·  Sponsor: Clinique du Sport, Bordeaux Mérignac

PhaseNA
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The mechanical alignment technique (Mechanical Alignment - MA) of a total knee prosthesis (TKA) was developed with the aim of making the installation of a TKA simple and reproducible, and that the prosthetic biomechanics are acceptable, thus promoting good longevity of implants. This is a technique that does not aim to restore the constitutional anatomy of the knee; bone cuts are systematically made at fixed angles, in the 3 planes of space, in relation to the mechanical axes of the long bones (femur and tibia). This non-personalized implantation technique therefore systematically alters the anatomy, laxity and kinematics of the knee, causing up to 50% of residual symptoms after prosthetic implantation and 20% of dissatisfied patients. In order to improve the clinical results of TKA, a new, more personalized and physiological technique was developed in 2007, called Kinematic Alignment (KA). This technique aims to restore the pre-arthritic anatomy, unique to each knee. Patients with severe constitutional deformity of the lower limb therefore retain this deformity after kinematic prosthetic replacement. The impact of the alignment technique on the biomechanics of the prosthetic knee remains poorly described. The main objective of this study is therefore to compare knee biomechanics between mechanical TKA and kinematic TKA.

This description comes directly from the study's public registry record.

Talk to the study team

Charles Rivière, MD  ·  +33 5 56 46 10 40  ·  charles.riviere@bari-arthroplasty.com

Always discuss trial participation with your own doctor first.

Locations (1)

Clinique du Sport Bordeaux MerignacMérignac, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06158646