Femoral Component TKA: Extramedullary vs Conventional Intramedullary Guide (EMAX (L2055))
Positioning Femoral Component TKA Using an Extramedullary Guide: Comparison With Conventional Intramedullary Guide
The study wants to evaluate the performance of this EM guide in comparison to a traditional IM guide.
75 patients will be included in the extramedullary group (to be compared with a corresponding previous group of 75 patients treated with intramedullary guide).
研究概览
地位
条件
详细说明
Total Knee Arthroplasty (TKA) is a widely performed surgical procedure aimed at relieving pain and restoring function in patients with advanced knee arthritis. The success of TKA is contingent upon precise implant positioning, particularly in relation to the femoral component. The femoral component's alignment significantly influences postoperative knee biomechanics, patient satisfaction, and long-term implant survival.
Conventional methods for femoral component positioning involve the use of intramedullary (IM) guides, which are inserted into the femoral canal to align the cutting block for bone preparation. While IM guides offer precise alignment, they can also lead to complications such as intraoperative fractures, fat embolism, activation of coagulation and excessive blood loss.
To address these limitations, extramedullary (EM) guides have emerged as an alternative option. EM guides are placed on the external surface of the femur without entering the medullary canal and avoiding complications that may occur reaming the canal.
In the recent past years, kinematic alignment (KA) has become widespread in use as a new technique for TKR that considers the patient's individual alignment and biomechanics. By restoring the pre-arthritic kinematic axes of the femur and tibia, KA aims to mimic the natural knee joint's function and movement.
In this study a specific EM guide - Anterior Cortex Stylus - is used to address the alignment of the femoral component in the context of a KA approach. The guide uses the anterior cortex of the distal femur as reference for cutting block positioning. The study aims to evaluate the performance of this EM guide in comparison to a traditional IM guide (used in previous group of patients).
This is an open, multi-centre, retro-prospective, observational, controlled study.
The primary aim is to evaluate whether the Anterior Cortex Stylus (in a retro-prospective collected series) is not inferior to the traditional intramedullary guide (previous group of patients) in term of positioning of the femoral component in TKA.
A total of 75 patients will be included in the extramedullary group (to be compared with a corresponding previous group of 75 patients treated with intramedullary guide). Both groups will be treated with a total knee arthroplasty using GMK Sphere (CE marked, class III) and a kinematic alignment approach.
研究类型
注册 (估计的)
联系人和位置
学习联系方式
- 姓名:Sara Zacchetti
- 电话号码:0039 0283502227
- 邮箱:sara.zacchetti@grupposandonato.it
研究联系人备份
- 姓名:Laura Mangiavini
- 电话号码:0039 0283502227
学习地点
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-
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Milan、意大利、20148
- 完全的
- Istituto Clinico San Siro
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Milan、意大利、20157
- 招聘中
- IRCCS Ospedale Galeazzi-Sant'Ambrogio [coordinator]
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接触:
- Zacchetti
- 电话号码:0039 0283502227
- 邮箱:sara.zacchetti@grupposandonato.it
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Torino、意大利、10152
- 完全的
- Ospedale Cottolengo
-
-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
取样方法
研究人群
The study shall include a total of 150 patients: 75 will be included in the extramedullary group, to be compared with a corresponding previous group of 75 patients treated with intramedullary guide. Patients meeting the inclusion criteria (mentioned below) will be recruited separately by each participating institution.
Patient enrolled in the retrospective analysis have been operated upon between January 2021 and September 2025.
描述
Inclusion Criteria:
- Male or female ≥ 18 years old
- Indication to primary TKA, for any diagnosis operated with EM or IM guides
- Signature of the informed consent (only for prospective cohort)
- Been operated upon between January 2021 and September 2025 (only for retrospective cohort)
Exclusion Criteria:
- Revision surgery of knee arthroplasty
- Patients with malignant diseases (at the time of surgery)
- Patients with proven or suspect infections (at the time of surgery)
- Pregnancy end/or lactating (auto declaration)
- Patient with known allergy to the specific metallic components of the prosthesis (at the time of surgery)
学习计划
研究是如何设计的?
设计细节
队列和干预
团体/队列 |
|---|
|
Extramedullary (EM) guides: Retroprospective + Prospective cohort
patients trated with extramedullary (EM) guides.
This cohort can be both Retroprospective and Prospective
|
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intramedullary (IM) guides: Retrospective cohort
patients trated with intramedullary (IM) guides.
This cohort will be only Retrospective
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Anterior Cortex Stylus
大体时间:Radiographic angle at 3 moth post-op in the sagittal plane, between the anterior cortex of the distal femur and the femoral component and compare it in the group operated with Anterior Cortex Stylus versus the group operated with IM guide.
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Radiographic angle at 3 moth post-op of the femoral component in TKA in an Anterior Cortex Stylus (retro-prospective collected series) compared to intramedullary guide (previous group of patients)
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Radiographic angle at 3 moth post-op in the sagittal plane, between the anterior cortex of the distal femur and the femoral component and compare it in the group operated with Anterior Cortex Stylus versus the group operated with IM guide.
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Results across study centres
大体时间:Compare the results in terms of radiographic sagittal angle between study centres at pre-op, surgery and 3 month post-op.
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Radiographic angles compared between the centres (at pre-op, surgery and 3 month post-op)
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Compare the results in terms of radiographic sagittal angle between study centres at pre-op, surgery and 3 month post-op.
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Adverse Events to determinate Instrument safety
大体时间:During surgery
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Number of: adverse events, adverse device effects, serious adverse events and serious adverse device effects
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During surgery
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合作者和调查者
调查人员
- 首席研究员:Corrado Sosio、Ospedale Galeazzi S.p.A.
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- EMAX (L2055)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
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研究美国 FDA 监管的设备产品
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