EUCTR2004-002824-16-SE进行中（未招募）不适用
Spinalt klonidin och baklofen som adjuvans till ryggmärgsstimulering vid terapiresistent smärta. (Möjlighet att förstärka den smärtlindrande effekten av alektrisk tyggmärgsstimulering med läkemedel som tillförs via ryggmärgskanalen)
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •1) Patients with neuropathic pain who have received a temporary electrode system for spinal cord stimulation, but experience pain reduction less than 50% or pain reduction not exeeding 45 minutes after completed spinal cord stimulation session.
- •2) Patients who previously have received a fully implanted system for spinal cord stimulation as a treatment for neuropathic pain, where pain-relief has diminished so that they now experience pain reduction less than 50% or pain reduction not exeeding 45 minutes after completed spinal cord stimulation session.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1) Mental handicap or other disturbance of communication.
- •2) Ongoing infection.
- •3) CNS disease
- •4) Heart- or other vascular disease.
- •5) Medication that may interact with the test substances.
研究者
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