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临床试验/NCT00921076
NCT00921076Unknown4 期

Gait Analysis of Patients Undergoing Total Ankle Arthroplasty, Ankle Arthrodesis, Tibiotalocalcaneal or Pantalar Fusion.

Unity Health Toronto2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2002年6月最近更新:
适应症

试验速览

阶段
4 期
入组人数
200
试验地点
2
主要终点
The primary outcome measure will be micro motion, consisting of component migration and rotation relative to the talus and distal tibia. This will be measured utilizing RSA with bi-planar stereo X-rays taken at several intervals: before weight bearing is

研究概览

简要总结

Surgical options for managing hindfoot arthritis include: joint fusion, total ankle joint replacement or osteotomies (realignment) of bones. Fusion of arthritic hindfoot joints has been the accepted method of managing hindfoot arthritis for over a century. Recently, total ankle replacement has evolved as a treatment option for patients with end stage ankle arthritis. A comparison of gait for patients before and after hindfoot fusion or total ankle replacement will give further information about the outcome of this treatment. The principal aim of this project is to assess the effect of total ankle replacement or hindfoot fusion on gait. We are also interested in the outcome of the surgery and its effect on your symptoms (eg. pain and mobility). The results of this study will aid researchers in assessing this new treatment modality. Your involvement in this study is critical for the researchers to further analyze this new form of treatment and your time and involvement is appreciated.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Symptomatic Ankle Arthritis
  • Skeletal maturity
  • Able to give informed consent

排除标准

  • Avascular Necrosis of Talus
  • Obesity (BMI >30)
  • Prior Ankle fusion or arthroplasty
  • Active or prior infection within 12 months
  • Medical condition precluding major surgery
  • Severe ipsilateral mid or hind foot deformity
  • Severe osteoporotic or osteopenic bone
  • Neuromuscular impairment
  • Age less than 40 years old
  • Cognitive or psychiatric impairment prohibiting accurate follow-up
  • Workers compensation board patients

结局指标

主要结局

The primary outcome measure will be micro motion, consisting of component migration and rotation relative to the talus and distal tibia. This will be measured utilizing RSA with bi-planar stereo X-rays taken at several intervals: before weight bearing is

时间窗: 12 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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