ACTRN12616001385437招募中1 期
Assessing feasibility, safety and efficacy of IVIg therapy in patients with acute traumatic spinal cord injury
niversity of Queensland0 个研究点目标入组 40 人开始时间: 2016年10月6日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
- 入组人数
- 40
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Non-randomised trial
- 主要目的
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 16 Years 至 o limit（—）
- 性别
- All
入选标准
- •Acute traumatic cervical or thoracic spinal cord injury (up to T9).
- •Initiation of IVIg treatment must be within 12 hours of injury.
排除标准
- •1.Known hypersensitivity to Privigen
- •2.History of significant cardiovascular, liver or kidney disease
- •3.Unconscious
- •4.Penetrating spinal cord injury
- •5.Involvement in another SCI research project
- •6.Presence of a mental disorder or other illness, which, in the view of the Principle Investigator (or their delegate) precludes informed consent and/or accurate medical evaluation.
- •7.Patients with history of regular substance abuse
- •8.Inability to commit or be available for follow-ups.
研究者
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