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临床试验/ISRCTN57950006
ISRCTN57950006进行中(未招募)4 期

Clinical and radiographic evaluation of the lumbar Scarlet AL-T cage outcomes within 24 months postoperatively

Spineart SA0 个研究点目标入组 100 人开始时间: 2023年3月9日最近更新:
适应症

试验速览

阶段
4 期
状态
进行中(未招募)
发起方
Spineart SA
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

性别
All

入选标准

  • 1. Age 18 years minimum
  • 2. Treated by interbody fusion with SCARLET®AL-T system
  • 3. Non opposition letter signed

排除标准

  • 1. Patient lacking capacity to follow postoperative care instructions due to mental state (suffering from dementia and others)
  • 2. Infection
  • 3. Severely damaged bone structures that could prevent stable implantation of the cage
  • 4. Neuromuscular or vascular disorders or illness
  • 5. Inadequate activity
  • 6. Pregnancy
  • 7. Bone tumor in the region of implant
  • 8. Fractures

研究者

发起方
Spineart SA

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