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Clinical and Radiological Impact of Tibial Cutting Int Total Knee Arthroplasty, Accelerated Navigation Versus Extramedullary Targeting

Primary Purpose

Gonarthrosis

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
First line total knee replacement for gonarthrosis .
Sponsored by
CHU de Reims
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Gonarthrosis focused on measuring Osteoarthritis Knee, Knee prosthesis, Patient satisfaction

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Gonarthrosis
  • Hip Knee Angle between 170° and 183°
  • Agreed to participate in the study

Exclusion Criteria:

  • Already undergone surgery on the same knee:

    • Uni-compartmental prosthesis
    • Total Knee Replacement
    • Tibial or femoral osteotomy for re-alignment
  • Vicious calls

Sites / Locations

  • Damien JOLLYRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Mechanical group

Gyroscopic group

Arm Description

Group of patients whose tibial sections will be performed using extramedullary mechanical sighting

Group whose tibial sections will be performed using gyroscopic and accelerometric navigation (I-Assist) will be randomized

Outcomes

Primary Outcome Measures

Achievement of the target tibial slope and the target tibial varus/valgus
Achievement of the target tibial slope of 3° +/- 2° and the target tibial varus/valgus +/- 2°. The tibial slope is defined by the angle (in degrees) between the mechanical axis of the tibia in profile and the tangent to the tibial cut. The tibial varus/valgus is the angle formed between the mechanical axis of the front tibia and the tangent to the tibial cut. This radiological evaluation is a usual assessment used in the follow-up of patients operated for a total knee replacement.

Secondary Outcome Measures

Achievement of target global coronal alignement
Achievement of the global coronal alignment target +/- 3° defined in the preoperative pase. Coronal alignment is defined by the HKA angle, the angle (in degrees) between the center of the femoral head, the center of the knee and the center of the tibio-fibluar mortise. This radiological evaluation is a usual assessment used in the follow-up of patients operated for a total knee replacement.
Patient satisfaction: New IKS score
Patient satisfaction will be assessed using the New International Knee Society score (New IKS score) collected by a blind investigator. The new IKS score was validated in French in 2014 (Debette C, Parratte S, Maucort-Boulch D, Blanc G, Pauly V, Lustig S, Servien E, Neyret P, Argenson JN. French adaptation of the new Knee Society Scoring System for total knee arthroplasty. Orthop Traumatol Surg Res. 2014 Sep;100(5):531-4.) New IKS score range from 0 to 200 with a physical score on 100 points (pain, knee' mobility, abnormal laxity, flexion deformity and Hips knee Ankle) and a functional score on 100 points (walking distance, difficulty with stairs and use of walking aids).

Full Information

First Posted
November 7, 2018
Last Updated
May 14, 2019
Sponsor
CHU de Reims
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1. Study Identification

Unique Protocol Identification Number
NCT03951545
Brief Title
Clinical and Radiological Impact of Tibial Cutting Int Total Knee Arthroplasty, Accelerated Navigation Versus Extramedullary Targeting
Official Title
Clinical and Radiological Impact of Tibial Cutting Int Total Knee Arthroplasty, Accelerated Navigation Versus Extramedullary Targeting : a Randomized Prospective Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2018
Overall Recruitment Status
Unknown status
Study Start Date
November 21, 2018 (Actual)
Primary Completion Date
February 21, 2021 (Anticipated)
Study Completion Date
August 21, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
CHU de Reims

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Type of study : Superiority study, comparative, randomized, double-blind (patient and evaluator will be blind from the randomization group), multicenter, prospective inclusion. Two groups of patients will be compared: a group of patients whose tibial sections will be performed using extramedullary mechanical sighting and a group whose tibial sections will be performed using gyroscopic and accelerometric navigation (I-Assist) will be randomized. Randomization will be performed with a 1/1 ratio per block. Population : Patients requiring 1st line total knee replacement for gonarthrosis with a Hip knee angle (HKA) between 170° and 183° who have agreed to participate in the study. Patients who have already undergone surgery on the same knee (uni-compartmental prosthesis, total knee replacement, tibial or femoral osteotomy for re-alignment, with the exception of arthroscopy) or who have vicious calls will not be included in the study. The number of subjects required was calculated using NQUERY 4.0 software for the main endpoint data, with the following assumptions: 51% of patients reaching the tibial cut target angles for the "extramedullary mechanical aiming" technique and 68% of patients reaching the tibial cut target angles for the I-Assist gyroscopic and accelerometric navigation technique. With an alpha risk of 5%, a power of 90%, and bilateral test, the number was estimated at 174 per group. Taking into account a percentage of included patients for whom total knee arthroplasty will not be performed of 10%, it is planned to include a total of 382 patients. Main judgment criteria : Achievement of the target tibial slope of 3°+/-2° and the target tibial varus/valgus at +/-2°. The tibial slope is defined by the angle (in degrees) between the mechanical axis of the tibia in profile and the tangent to the tibial cut. The varus/valgus tibial is the angle formed between the mechanical axis of the front tibia and the tangent to the tibial cut. Investigation plan : Proposal to participate in the research to any eligible patient at the time of a preoperative consultation with the orthopaedic surgeon. If the patient agrees to participate in the research (signature of the informed consent form), a randomization will be performed to determine the group of bone cutting technique. The patient will be blind to the result of randomization. The clinical follow-up of the patient will not be modified by the study, with as usual: A 6-week consultation with interrogation, clinical and radiographic examination (Face and profil x-rays, axial patella views) A 3-month consultation with interrogation, clinical and radiographic examination (Face and profil x-rays, axial patella views, telemetry of the lower limbs in charge and full profile leg x-rays). Measurements of the radiographic judgement criteria will be performed by two orthopaedic surgeons and a blind radiologist of the cutting technique used. The tibial slope will be analyzed on the entire leg radiograph in profile at 3 months. Coronal alignment will be studied on telemetry of the front lower limbs loaded at 3 months. Joint amplitudes and patient satisfaction will be assessed at 3 months postoperatively with the New IKS score, by a blind surgeon of the surgical technique used. Statistical analysis plan : Comparison of the characteristics of the 2 groups Analysis of the main endpoint: comparison of the percentage of patients with the target tibial slope achieved in both groups by Chi2 test or an accurate Fisher test, depending on the application conditions. Analysis of secondary judgment criteria by Student, Wilconxon, Chi2 or exact Fisher tests, depending on the application conditions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gonarthrosis
Keywords
Osteoarthritis Knee, Knee prosthesis, Patient satisfaction

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
382 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mechanical group
Arm Type
Active Comparator
Arm Description
Group of patients whose tibial sections will be performed using extramedullary mechanical sighting
Arm Title
Gyroscopic group
Arm Type
Experimental
Arm Description
Group whose tibial sections will be performed using gyroscopic and accelerometric navigation (I-Assist) will be randomized
Intervention Type
Procedure
Intervention Name(s)
First line total knee replacement for gonarthrosis .
Intervention Description
Patients requiring 1st line total knee replacement for gonarthrosis with a Hip knee angle (HKA) between 170° and 183°. In the first group (Mechanical) the total knee replacement will be performed with a tibial cut by using extramedullary mechanical sighting and in the second group (Gyroscopic) by using gyroscopic and accelerometric navigation (I-Assist).
Primary Outcome Measure Information:
Title
Achievement of the target tibial slope and the target tibial varus/valgus
Description
Achievement of the target tibial slope of 3° +/- 2° and the target tibial varus/valgus +/- 2°. The tibial slope is defined by the angle (in degrees) between the mechanical axis of the tibia in profile and the tangent to the tibial cut. The tibial varus/valgus is the angle formed between the mechanical axis of the front tibia and the tangent to the tibial cut. This radiological evaluation is a usual assessment used in the follow-up of patients operated for a total knee replacement.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Achievement of target global coronal alignement
Description
Achievement of the global coronal alignment target +/- 3° defined in the preoperative pase. Coronal alignment is defined by the HKA angle, the angle (in degrees) between the center of the femoral head, the center of the knee and the center of the tibio-fibluar mortise. This radiological evaluation is a usual assessment used in the follow-up of patients operated for a total knee replacement.
Time Frame
3 months
Title
Patient satisfaction: New IKS score
Description
Patient satisfaction will be assessed using the New International Knee Society score (New IKS score) collected by a blind investigator. The new IKS score was validated in French in 2014 (Debette C, Parratte S, Maucort-Boulch D, Blanc G, Pauly V, Lustig S, Servien E, Neyret P, Argenson JN. French adaptation of the new Knee Society Scoring System for total knee arthroplasty. Orthop Traumatol Surg Res. 2014 Sep;100(5):531-4.) New IKS score range from 0 to 200 with a physical score on 100 points (pain, knee' mobility, abnormal laxity, flexion deformity and Hips knee Ankle) and a functional score on 100 points (walking distance, difficulty with stairs and use of walking aids).
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Gonarthrosis Hip Knee Angle between 170° and 183° Agreed to participate in the study Exclusion Criteria: Already undergone surgery on the same knee: Uni-compartmental prosthesis Total Knee Replacement Tibial or femoral osteotomy for re-alignment Vicious calls
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Renaud SIBONI
Phone
03 26 78 88 85
Ext
0033
Email
rsibony@chu-reims.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Guillaume BRESSY
Email
dr.gbressy@gmail.com
Facility Information:
Facility Name
Damien JOLLY
City
Reims
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Renaud SIBONI
Phone
03 26 78 88 85
Ext
0033
Email
rsiboni@chu-reims.fr

12. IPD Sharing Statement

Learn more about this trial

Clinical and Radiological Impact of Tibial Cutting Int Total Knee Arthroplasty, Accelerated Navigation Versus Extramedullary Targeting

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