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KBARS Study: The effect of knee prosthesis design on knee biomechanics during locomotion following knee replacement surgery

KBARS Study: The effect of knee prosthesis design on knee biomechanics during locomotion following knee replacement surgery

Status
Completed
Phases
Unknown
Study type
Observational
Source
ANZCTR
Registry ID
ACTRN12616000604404
Acronym
KBARS
Enrollment
72
Registered
2016-05-10
Start date
2016-04-26
Completion date
2017-04-04
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

The purpose of this study is to determine if knee movement and muscle activity of patients implanted with a medial pivot prosthesis design is more normal compared to crucial-retaining or posterior-stabilized designs during locomotion.

Interventions

1. Patients implanted with a medial pivot prosthesis design, an cruciate sacrificing design characterised by high-conformity in the medial compartment (socket on the insert, as well as anterior and posterior lips to prevent femoral translation) and a flatter tibial surface on the lateral side to facilitate tibiofemoral rotation with an axis located on the medial side. Alternative designs such as cruciate-retaining (CR) do not feature medial-lateral differences in geometry and retain the posterio

1. Patients implanted with a medial pivot prosthesis design, an cruciate sacrificing design characterised by high-conformity in the medial compartment (socket on the insert, as well as anterior and posterior lips to prevent femoral translation) and a flatter tibial surface on the lateral side to facilitate tibiofemoral rotation with an axis located on the medial side. Alternative designs such as cruciate-retaining (CR) do not feature medial-lateral differences in geometry and retain the posterior-cruciate ligament. Posterior stabilized knees (PS) also sacrifice the cruciate ligaments, but maintain stability through a post and cam system. 2. Each participant will be followed up for a one-hour session at a minimum follow-up of 12months post knee replacement surgery.

Sponsors

Sydney Orthopaedic Research Institute
Lead SponsorCharities/Societies/Foundations

Eligibility

Sex/Gender
All
Age
45 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

Patients receiving a knee replacement a minimum of 12months prior to testing BMI <35kg/m2 Able to walk on a treadmill for >120sec; step up/down on a 20cm step

Exclusion criteria

Primary language other than English Pregnant women Children or young adults Persons diagnosed with neurological disorders that would preclude safely performing locomotion in a laboratory environment Persons with intellectual or mental impairments People highly dependent on medical care

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026