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临床试验/NCT01284998
NCT01284998已完成不适用

Short Term Follow-up of Patent Implanted With the B-BOP Lock Plate

Integra LifeSciences Services3 个研究点 分布在 3 个国家目标入组 85 人开始时间: 2009年6月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
85
试验地点
3
主要终点
Rate of device related complications.

研究概览

简要总结

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.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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

结局指标

主要结局

Rate of device related complications.

时间窗: 12 months

Iprovement of American Orthopaedic Foot and Ankle Society Hallux Metatarsophalangeal-lnterphalangeal Scale (AOFAS HMIS) score

时间窗: 12 months

次要结局

  • X rays evaluation(3 and12 months)
  • Pain using a visual analog scale(3 and 12 months)
  • Function assessment(3 and 12 Months)
  • Clinical assessment(3 and 12 months)

研究者

发起方
Integra LifeSciences Services
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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