ATTUNE TM Video-fluoroscopy Study
Kinematics Analysis: Cruciate Retaining, Fixed Bearing Primary Total Knee Arthroplasty With the ATTUNE TM Knee System
1 other identifier
observational
5
1 country
1
Brief Summary
The proposed study is a retrospective, observational study. A group of 5 subjects with the AttuneTM cruciate retaining (CR) fixed bearing total knee arthroplasty (TKA) are analysed during level walking, a deep knee bend, sitting down onto a chair, standing up from a chair and stair descent at least 12 months post-operatively, in terms of 3D fluoroscopic assessed tibio-femoral TKA motion as well as simultaneous skin marker assessed whole leg motion and ground reaction forces. The obtained information helps the manufacturer (DePuy) to evaluate, bring to market and advance the implant. Furthermore the information will be integrated in a model, which will be developed at the Center for Orthopaedic Engineering, University of Denver. By means of this model, different conditions such as the use of an advanced prosthesis design can be simulated and tested. The objective of this study is in a first step to demonstrate the capability of data collection and analysis of level gait, deep knee bend, sitting down onto a chair, standing up from a chair and stair descent on a limited sample size of five subjects. Secondly to quantify and describe the three-dimensional kinematics for the cruciate retaining (CR), fixed bearing AttuneTM TKA during daily activities such as those mentioned.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for all trials
Started Jul 2015
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
February 4, 2015
CompletedFirst Posted
Study publicly available on registry
February 9, 2015
CompletedStudy Start
First participant enrolled
July 1, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
September 1, 2016
CompletedJanuary 26, 2017
January 1, 2017
8 months
February 4, 2015
January 25, 2017
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Relationship between the knee flexion angle and the medial and lateral anterior-posterior translation of the condyles
The primary outcome of this pilot study is the relationship between the knee flexion angle and the medial and lateral anterior-posterior translation of the condyles during level walking, stair descent, standing up from a chair, sitting onto a chair and deep knee bend.
3 hours
Interventions
Eligibility Criteria
Prof. Dr. med. Carsten Perka will do the recruitment, since he is the surgeon that worked the most with this implant and therefore also has the biggest population of possibly eligible patients. Furthermore the patients already know and trust him, which could lead to a greater success in the recruitment as well. For these reasons the financial source DePuy Synthes, Johnson and Johnson, requires that the clinical collaborator Prof. Dr. med. Carsten Perka will do the recruitment. He works in the Charité in Berlin, Germany, where he does the recruitment.
You may qualify if:
- Unilateral TKA (ATTUNETM) due to osteoarthrosis (OA)
- Body mass index (BMI) ≤ 33
- Good clinical outcome, Knee injury and Osteoarthritis Outcome Score (KOOS) \> 70
- No or very low Visual Analog Scale for Pain (VAS) \< 2
- At least one year post-op
- Standardized general health survey score (SF-12) within the normal range for people in their age group
You may not qualify if:
- Actual significant problem on lower extremities
- Misaligned TKA
- Any other arthroplasty at the lower extremities
- Patient incapable to understand and sign informed consent
- Incapable of performing the motion tasks
- Pregnancy
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Dr. Renate Listlead
Study Sites (1)
Institute for Biomechanics
Zurich, Canton of Zurich, 8093, Switzerland
Study Officials
- PRINCIPAL INVESTIGATOR
Renate List, PhD
ETH Zurich
Study Design
- Study Type
- observational
- Observational Model
- CASE CONTROL
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Dr. sc. ETH Zurich
Study Record Dates
First Submitted
February 4, 2015
First Posted
February 9, 2015
Study Start
July 1, 2015
Primary Completion
March 1, 2016
Study Completion
September 1, 2016
Last Updated
January 26, 2017
Record last verified: 2017-01