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临床试验/NCT00150683
NCT00150683已完成不适用

Evaluation of Conventional and Innovative Standing Frame for the Treatment of Osteoporosis After Spinal Cord Injury

Toronto Rehabilitation Institute2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 1999年3月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
60
试验地点
2
主要终点
Change in bone mineral density from baseline of the hip, distal femur and proximal tibia at 6-months and 12-months.

研究概览

简要总结

The purpose of this study is to find out if standing and/or standing with vibration works for the treatment of osteoporosis for people with a spinal cord injury.

研究设计

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

入排标准

年龄范围
16 Years 至 80 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Traumatic spinal cord injury of greater than 12 months.
  • Osteopenia or osteoporosis of the hip.

排除标准

  • Pregnant or lactating females.
  • Nonunion lower extremity fracture within the last 6 months.
  • Bilateral hip or knee flexion contractures.
  • Bilateral lower extremity total hip or knee replacement.
  • Heterotopic ossification of the hip or knee.
  • Concurrent treatment with a bisphosphonate.

结局指标

主要结局

Change in bone mineral density from baseline of the hip, distal femur and proximal tibia at 6-months and 12-months.

次要结局

  • Spasticity (modified Ashworth).
  • Quality of life.
  • Frequency and severity of adverse events.

研究者

申办方类型
Other

研究点 (2)

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