NL-OMON42734尚未招募不适用
Quantitative Sensory Testing and Conditioned Pain Modulation in patients after cervical percutaneous cordotomy - QST and CPM after cordotomy
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 10
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
- 年龄范围
- 18 至 99（—）
入选标准
- •-Cervical percutaneous cordotomy, 2-4 weeks prior to the sensory testing
- •-The cervical percutaneous cordotomy must have been successfull: a loss of vital sensibility (determined by a positive pin-prick: a sharp pinch applied with a paper clip) caudal to dermatome C5, contralateral to the cordotomy side.
- •-Informed consent must have been obtained
排除标准
- •-Neurological disease/ nerve conduction disorder, which will influence the results of a bilateral QST measurement
- •-Inability to understand and speak in dutch
- •-When the sensory testing will be too much of a burden for the patient (in terms of psychological capacity, logistic problems, or a very limited prognosis). The attending Anesthesiologist/Pain Specialist (P. Zomers) will determine this.
研究者
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