NCT02358434

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
5

participants targeted

Target at below P25 for all trials

Timeline
Completed

Started Jul 2015

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 4, 2015

Completed
5 days until next milestone

First Posted

Study publicly available on registry

February 9, 2015

Completed
5 months until next milestone

Study Start

First participant enrolled

July 1, 2015

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2016

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2016

Completed
Last Updated

January 26, 2017

Status Verified

January 1, 2017

Enrollment Period

8 months

First QC Date

February 4, 2015

Last Update Submit

January 25, 2017

Conditions

Keywords

Implant

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

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Institute for Biomechanics

Zurich, Canton of Zurich, 8093, Switzerland

Location

Study Officials

  • Renate List, PhD

    ETH Zurich

    PRINCIPAL INVESTIGATOR

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

Locations