跳至主要内容
临床试验/NCT06835868
NCT06835868招募中不适用

Nationwide Dynamic Register for Screening, Evaluation and Follow-up of Patients Suffering from Chronic Pain Syndromes and Treated by Means of Invasive Neuromodulation.

University Hospital, Antwerp1 个研究点 分布在 1 个国家目标入组 7,000 人开始时间: 2018年2月14日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
7,000
试验地点
1
主要终点
Pain intensity after 21 days

研究概览

简要总结

Patients suffereing from chronic pain due to persistent spinal pain syndromes or complex regional pain syndromes and living in Belgium will be included in this register once they are being considered for a treatment with invasive neuromodulation (either spinal cord stimulation either dorsal root ganglion stimulation). The screening process, the multidisciplinary evaluation, the trial therapy and the long-terl follow-up will be monitored through this register.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • chronic pain syndromes

排除标准

  • acute pain syndromes

结局指标

主要结局

Pain intensity after 21 days

时间窗: 21 days

Follow-up of pain intensity (measured by the Numeric Rating Scale, with a minimum of 0 and a maximum score of 10) during the trial therapy of 21 days, together with quality of sleep and quality of ambulation (also ona NRS scale from 0 to 10).

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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