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Gait Kinematics After Primary Total Knee Arthroplasty (TKA) Versus Revision TKA

Assessment at Short Term of the Gait Kinematics After Primary TKA (Stryker) Versus After Revision TKA. Prospective and Controlled Study.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03898544
Acronym
Stryker-KneeKG
Enrollment
32
Registered
2019-04-02
Start date
2019-03-18
Completion date
2020-09-10
Last updated
2021-04-08

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

Conditions

Gait Analysis, Knee Arthroplasty, Total

Keywords

gait kinematics, TKA

Brief summary

The functional outcomes after TKA are satisfying with a full recovery at 6 months - 1 year. Nevertheless, the revisions of TKA have often lower functional results than primary TKA with a long delay of recovery. The Stryker TKA present the same device for primary TKA and for revision. The aim of this study is to compare the gait kinematics at 6 months after primary Stryker TKA or Revision Stryker TKA to assess if the objective outcomes are similar with this device.

Interventions

DEVICEGroup primary TKA

Assessment by gait kinematics analysis The total knee arthroplasty will be performed as usual with the dedicated instrumentation. The gait kinematics analysis will be performed with the KneeKG system on a treadmill, with infrared sensors (IR) on the leg. This system is not invasive. The IR sensors are positioned on the pelvis, the distal femur and the tibial crest. This system records the flexion/extension, the varus/valgus and the rotation during the walking (1 minute of walking).

DEVICEGroup TKA revision

Assessment by gait kinematics analysis The total knee arthroplasty will be performed as usual with the dedicated instrumentation. The gait kinematics analysis will be performed with the KneeKG system on a treadmill, with infrared sensors on the leg. This system is not invasive. The IR sensors are positioned on the pelvis, the distal femur and the tibial crest. This system records the flexion/extension, the varus/valgus and the rotation during the walking (1 minute of walking).

Sponsors

Stryker Nordic
CollaboratorINDUSTRY
Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Primary TKA group: symptomatic femorotibial osteoarthritis, with an indication of primary TKA (as Triathlon Stryker) * Revision group: first TKA removal in 1 step for mechanical failure, by a revision TKA (as Triathlon Stryker)

Exclusion criteria

* Septic failure * Second or more failure in the revision group * Associated surgical procedure as osteotomy, allograft… * Not full weight bearing postoperatively * Refusal to participate

Design outcomes

Primary

MeasureTime frameDescription
Femorotibial mechanical axis (varus, valgus) analysisat 6 months postoperativelyThese parameters are measured with the KneeKG system during the walking
range of motion (flexion, extension) analysisat 6 months postoperativelyThese parameters are measured with the KneeKG system during the walking
internal/external rotation analysisat 6 months postoperativelyThese parameter is measured with the KneeKG system during the walking
Walking speedat 6 months postoperativelyThese parameter is measured with the KneeKG system

Countries

France

Outcome results

None listed

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