Short Term Follow-up of Patent Implanted With the B-BOP Lock Plate
In case of deformities of the forefoot (Hallux-valgus, Hallux-varus), the basal osteotomy may be more indicated than the distal osteotomy as it allows to achieve a greater degree of correction.
However, weight bearing forces on the head of the first metatarsal acting at a distance from the osteotomy site subject the construct to an important dorsiflexion stress. Fixation strength being the important consideration led to design the B-BOP® Lock plate, specifically dedicated to basal osteotomy of the first metatarsal, with the following characteristics:
- plantar positioning to obtain the best stability and resistance while reducing the implant bulkiness;
- anatomical shape adapted to the plantar curve of the first metatarsal. Taking advantages of the most appropriated anatomical site to implant the B-BOP® Lock plate directly on tension, it offers an innovative and unique basal osteotomy fixation solution.
The B-BOP® Lock osteosynthesis plate benefits now of the Surfix locking screws technology.
The purpose of this study is to collect and publish data from several centers, several users.
研究概览
地位
研究类型
注册 (实际的)
联系人和位置
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
取样方法
研究人群
描述
Inclusion Criteria:
- Subject of either gender who needs a fixation of osteotomy of the basis of the first metatarsal for whose surgeon has recommended that a B-BOP® Lock plate from INTEGRA be implanted can be enrolled in this study.
- Age ≥ 18 years
- Have willingness to give his/her data transfer authorisation
Exclusion Criteria:
- Contraindication of the implantation of the B-BOP Lock plate
- History of prior mental illness or patient demonstrates that their mental capacity may interfere with their ability to follow the study protocol
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 |
|---|
|
B-BOP lock
Subjects who needs a fixation of osteotomy of the basis of the first metatarsal and for whose surgeon has recommended that a B-BOP® Lock plate from INTEGRA be implanted can be enrolled in this study
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Rate of device related complications.
大体时间:12 months
|
12 months
|
|
Iprovement of American Orthopaedic Foot and Ankle Society Hallux Metatarsophalangeal-lnterphalangeal Scale (AOFAS HMIS) score
大体时间:12 months
|
12 months
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
X rays evaluation
大体时间:3 and12 months
|
3 and12 months
|
|
Pain using a visual analog scale
大体时间:3 and 12 months
|
3 and 12 months
|
|
Function assessment
大体时间:3 and 12 Months
|
3 and 12 Months
|
|
Clinical assessment
大体时间:3 and 12 months
|
3 and 12 months
|
合作者和调查者
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
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
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