NCT02902627已完成不适用
Pain in Oncolgy: Evaluation of a Non Invasive Monitoring Device (ANI). A Monocentric Prospective Study
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- Hopital Foch
- 入组人数
- 80
- 试验地点
- 2
- 主要终点
- Comparison of the ANI parameter with the VAS
研究概览
简要总结
l'ANI (Analgesia Nociception Index
The main objective of the research is to estimate the Analgesia Nociception Index (ANI) as a parameter giving the possibility of measuring the pain in painful metastatic cancer. The parameter ANI is compared with visual analogical scale (VAS) score.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •more than 18 years, -no legal protection, -
- •life expectancy is considered over 3-months
- •not receiving of béta-blocking,
- •Having a rhythm sinusal without extrasystole
- •benefiting from a coverage by a social security system
排除标准
- •Pace-Maker
- •Diabetes mellitus
研究组 & 干预措施
Metastatic cancer
Experimental
干预措施: Non Invasive Monitoring Device (ANI) (Device)
结局指标
主要结局
Comparison of the ANI parameter with the VAS
时间窗: 4 hours
次要结局
未报告次要终点
研究者
研究点 (2)
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