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临床试验/NCT03439904
NCT03439904Unknown不适用

Impact of Individualized Pharmaceutical-care on Medication Adherence and Outcome of Cancer Pain in Opioid-tolerant Outpatients

Zhejiang Cancer Hospital1 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年6月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
200
试验地点
1
主要终点
Change in medication adherence

研究概览

简要总结

The purpose of the study is to investigate the impact of pharmaceutical care on cancer pain treatment for opioid-tolerant outpatients

详细描述

This study is a prospective multicenter randomized controlled study to investigate the impact of pharmaceutical care on cancer pain treatment for opioid-tolerant outpatients treated with sustained released morphine, oxycodone, and transdermal fentanyl.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
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

入选标准

  • Patients aged 18 years or older;
  • Histologically confirmed solid tumor;
  • Diagnosed chronic cancer pain;
  • Opioid-tolerant patients;
  • Overall survival is expected to be over 3 months;
  • Karnofsky performance score≥50;
  • Willing and able to comply with the protocol

排除标准

  • Patients aged 18 years or older;
  • Histologically confirmed solid tumor;
  • Diagnosed chronic cancer pain;
  • Opioid-tolerant patients;
  • Overall survival is expected to be over 3 months;
  • Karnofsky performance score≥50;
  • Willing and able to comply with the protocol

研究组 & 干预措施

pharmaceutical care intervention group

Experimental

Patients will receive individualized pharmaceutical care in addition to usual medical care

干预措施: Pharmaceutical care (Other)

control group

No Intervention

Patients will receive usual medical care

结局指标

主要结局

Change in medication adherence

时间窗: Change from baseline at 1 month

The investigators will measure the change in medication adherence via Morisky Scale from baseline to 1 months. Morisky Scale contains 4 questions, and the total score ranges from 0 to 4 with lower scores indicating higher adherence.

次要结局

  • Change in pain score(Change from baseline pain score at 1 month)
  • Change in quality of life(Change from baseline quality of life at 1 month)
  • Change in patients' knowledge of cancer pain and analgesics(Change from baseline knowledge at 1 month)
  • Incidence of adverse events [safety and tolerability](Up to 1 month)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ping Huang

Chief of Pharmacy

Zhejiang Cancer Hospital

研究点 (1)

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