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Axial Alignment in Patients Operated Using the Visionaire Patient Matched Cutting Blocks (Visionaire)

Primary Purpose

Osteoarthritis of the Knee

Status
Terminated
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
Visionaire
Standard surgical technique
Sponsored by
Smith & Nephew Orthopaedics AG
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Osteoarthritis of the Knee focused on measuring Randomized Controlled Trial, Total Knee Arthroplasty, Patient Matched Cutting Blocks

Eligibility Criteria

40 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Indication for TKA, Axial alignment between 10 degrees valgus and 20 degrees varus, BMI <36, patient must be amendable for both Genesis II total knee and Visioniare cutting blocks

Exclusion Criteria:

  • Insufficient femoral or tibia bone stock, inflammatory arthritis (e.g. rheumatoid arthritis), patient is immunosuppressed, has an active infection (local or systemic), patient has physical, emotional or neurological conditions that would compromise the patients compliance with rehabilitation and follow up.

Sites / Locations

  • Leicester General Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Visionaire

Standard Surgical technique

Arm Description

the group who will be operated by the use of Visionaire patient matched cutting blocks

The group who will be operated by means fo standard surgical technique

Outcomes

Primary Outcome Measures

Axial Alignment
Axial alignment will be measured by means of CT scan and long leg x-ray

Secondary Outcome Measures

Clinical effectiveness and safety.
Safety and effectiveness will be measured by means of Knee Society Score, Oxford Score, EQ-5D and radiographic findings

Full Information

First Posted
October 14, 2010
Last Updated
April 13, 2015
Sponsor
Smith & Nephew Orthopaedics AG
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1. Study Identification

Unique Protocol Identification Number
NCT01224522
Brief Title
Axial Alignment in Patients Operated Using the Visionaire Patient Matched Cutting Blocks
Acronym
Visionaire
Official Title
PATIENT-MATCHED INSTRUMENTATION Versus (vs) STANDARD INSTRUMENTATION: A RANDOMIZED CLINICAL TRIAL COMPARING POSTOPERATIVE AXIAL ALIGNMENT and COMPONENT POSITION
Study Type
Interventional

2. Study Status

Record Verification Date
April 2015
Overall Recruitment Status
Terminated
Why Stopped
protocol deviations
Study Start Date
March 2011 (undefined)
Primary Completion Date
August 2014 (Actual)
Study Completion Date
August 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Smith & Nephew Orthopaedics AG

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
- Title: PATIENT-MATCHED INSTRUMENTATION VS. STANDARD INSTRUMENTATION: A RANDOMIZED CLINICAL TRIAL COMPARING POSTOPERATIVE AXIAL ALIGNMENT and COMPONENT POSITION Short Title: Visionaire Alignment Methodology: Monocentric, Single Blinded, Randomized Controlled Trial Study Duration: November 2010 to July 2014 Study Centres: Leicester General Hospital, United Kingdom (UK)
Detailed Description
Malalignment is one of the main reasons for knee arthroplasty revision. With the use of patient matched cutting block we expect better axial alignment of the components. Research Objectives: The primary research objective is to evaluate the axial alignment and component position in TKA with use of Smith & Nephew's VISIONAIRE Patient Matched Technology and to compare with the alignment when standard instrumentation. Secondary research objectives include assessing the safety and effectiveness of the VISIONAIRE patient matched technology as compared to commonly accepted standard instrumentation in patients suffering from symptomatic osteoarthritis of the knee joint. - Outcome Measures: Implant alignment and Component position by means of CT-scans Knee Society Score EuroQol-5 Dimensions (EQ-5D) Knee injury and Osteoarthritis Outcome Score (KOOS) Oxford Knee Score Knee-related adverse events Standard and full leg x-ray Number of Subjects: 70 (2*35) Enrollment time: 18 months Diagnosis and Main Inclusion Criteria: Patients with osteoarthritis of the knee requiring total knee arthroplasty Study Product, Dose, Route, Regimen: VISIONAIRE patient matched technology versus the commonly accepted standard instrumentation for the Genesis II total knee arthroplasty implant

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Osteoarthritis of the Knee
Keywords
Randomized Controlled Trial, Total Knee Arthroplasty, Patient Matched Cutting Blocks

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
70 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Visionaire
Arm Type
Experimental
Arm Description
the group who will be operated by the use of Visionaire patient matched cutting blocks
Arm Title
Standard Surgical technique
Arm Type
Active Comparator
Arm Description
The group who will be operated by means fo standard surgical technique
Intervention Type
Procedure
Intervention Name(s)
Visionaire
Other Intervention Name(s)
Standard Smith & Nephew instruments, Visionaire Instruments
Intervention Description
Implantation of a Genesis II Total Knee by means of Visionaire patient matched cutting blocks.
Intervention Type
Procedure
Intervention Name(s)
Standard surgical technique
Intervention Description
Implantation of Genesis II Total Knee system by means of standard surgical technique.
Primary Outcome Measure Information:
Title
Axial Alignment
Description
Axial alignment will be measured by means of CT scan and long leg x-ray
Time Frame
6 weeks,
Secondary Outcome Measure Information:
Title
Clinical effectiveness and safety.
Description
Safety and effectiveness will be measured by means of Knee Society Score, Oxford Score, EQ-5D and radiographic findings
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Indication for TKA, Axial alignment between 10 degrees valgus and 20 degrees varus, BMI <36, patient must be amendable for both Genesis II total knee and Visioniare cutting blocks Exclusion Criteria: Insufficient femoral or tibia bone stock, inflammatory arthritis (e.g. rheumatoid arthritis), patient is immunosuppressed, has an active infection (local or systemic), patient has physical, emotional or neurological conditions that would compromise the patients compliance with rehabilitation and follow up.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Urjit Chatterji, MD
Organizational Affiliation
Leicester General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Leicester General Hospital
City
Leicester
ZIP/Postal Code
LE5 4PW
Country
United Kingdom

12. IPD Sharing Statement

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Axial Alignment in Patients Operated Using the Visionaire Patient Matched Cutting Blocks

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