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临床试验/NCT04491123
NCT04491123已完成不适用

Evaluation of Discomfort Symptoms in Patients With Refractory Cancer Pain and Intrathecal Analgesia Management

University Hospital, Montpellier1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2018年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
1
主要终点
Number Evaluation of Edmonton symptoms

研究概览

简要总结

Intrathecal analgesia is used in refractory cancer pain because of drug sides effects or intractable pain. The aim of this approach is to improve pain management, and also to improve patient comfort. This study will assess patient discomfort symptoms before and after setting up intrathecal analgesia.

详细描述

Descriptive multicenter study including patients with refractory cancer pain (unmanageable drug sides effects or intractable pain) who will receive intrathecal analgesia Patient discomfort symptoms will be evaluated before and after the beginning of intrathecal analgesia at 15, 30, 60 and 90 days.

Moreover, the impact on patient close relatives and on return home will be assessed.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

结局指标

主要结局

Number Evaluation of Edmonton symptoms

时间窗: up to 90 days after patient inclusion

Edmonton symptom assessment system

次要结局

  • Autonomy assessment score for activities of daily living(1 day)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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