相关药物
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 入组人数
- 106
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •- Patients with sciatica of disc origin (radio-clinical concordance on MRI or CT) postero-lateral
- •- Duration of evolution greater than 3 weeks despite analgesic / NSAID treatment, and less than 3 months
- •- EVA sciatic pain > 4/10
- •- Oswestry greater than or equal to 30 at inclusion
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) no
- •F.1.2.1 Number of subjects for this age range 90
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range 16
排除标准
- •- Signs or risks of infection, in particular signs of viral infection (perform a screening PCR if there is any doubt that it is still a pandemic period when the protocol is set up)
- •- Poor local skin condition
- •- Anticoagulation with VKA or anti-Xa, or haemorrhagic disease (authorised antiaggregants)*.
- •- Neurological deficit < 3/5 or signs of cauda equina irritation
- •- Tarlov's cyst or low dural sac below S4
- •- Allergy to Lidocaine, Dexamethasone or Sulphites
- •- Spinal infiltration in the previous 3 months
- •- Patient with bilateral sciatica
- •- Patient with sciatica of arthritic origin
- •- Patient with chronic respiratory failure
研究者
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