A Study Of ATTUNE CR TKA WITH MEDIAL STABILIZATION TKA

Overview

About this study

The purpose of this study is to determine in vivo, weight-bearing kinematics for subjects with either a DePuy Attune CR TKA or a DePuy Attune CR TKA with a Medial Stabilized (MS) insert, implanted using multiple different alignment techniques. This will involve a fluoroscopic analysis to determine the in vivo kinematics, inverse modeling to determine the in vivo kinetics, and patient outcome surveys to determine clinical outcomes.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

1. Age range of 18 years to 85 years (both inclusive)

2. Must be at least 6 months post-operative

3. Must be able to safely perform the requested activity

4. Must have the appropriate TKA systems

Exclusion Criteria:

1. Pregnant, potentially pregnant, or lactating females. To satisfy radiation protocols, all potential female subjects will be asked if they are pregnant or could possibly be pregnant.

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

 

Eligibility last updated 09/24/2025. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Kevin Perry

Open for enrollment

Contact information:

Matthew Hoplin

(507) 284-1003

Hoplin.Matthew@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20597482

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