Survivorship and Outcomes of Robot Assisted Medial Partial Knee Replacement

NCT ID: NCT01845597

Last Updated: 2023-07-13

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

145 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-04-30

Study Completion Date

2022-02-28

Brief Summary

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The purpose of this study is to determine the survivorship rate of robotic assisted medial partial knee replacement at a two, five, and ten years.

Detailed Description

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The purpose of this study is to determine the survivorship rate of robotically guided MultiCompartmental Knee system (MCK) medial onlay Unicompartmental Knee Arthroplasty (UKA) implants at a two, five, and ten year follow up.

Conditions

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Unicompartmental Knee Arthroplasty

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Study Groups

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MAKOplasty® medial UKA

Patients knees that have received a MAKOplasty® robotically guided unicompartmental knee arthroplasty (UKA) and received a medial MCK onlay implant.

MAKOplasty® medial UKA

Intervention Type PROCEDURE

A robot guided medial Unicompartmental knee arthroplasty (UKA) is a procedure to replace only the medial tibiofemoral compartment of the knee.

Interventions

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MAKOplasty® medial UKA

A robot guided medial Unicompartmental knee arthroplasty (UKA) is a procedure to replace only the medial tibiofemoral compartment of the knee.

Intervention Type PROCEDURE

Other Intervention Names

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Medial Partial Knee Replacement Medial Unilateral Knee Arthroplasty Robot Assisted Partial Knee Replacement

Eligibility Criteria

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Inclusion Criteria

* over 21 years of age
* underwent primary robotically guided UKA and received a medial MCK onlay implant by the investigating surgeon
* at least 24 months post-operative

Exclusion Criteria

* Patients will be excluded from participation in the study if they are cognitively unable to answer study questions
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stryker Instruments

INDUSTRY

Sponsor Role collaborator

Northwest Surgical Specialists, Vancouver

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Todd Borus, MD

Role: PRINCIPAL_INVESTIGATOR

Rebound Orthopedics and Neurosurgery

Locations

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Rebound Orthopedics and Neurosurgery

Vancouver, Washington, United States

Site Status

Countries

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United States

Provided Documents

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Document Type: Study Protocol

View Document

Other Identifiers

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2016-006

Identifier Type: OTHER

Identifier Source: secondary_id

MAKO-03

Identifier Type: -

Identifier Source: org_study_id

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