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临床试验/NCT03455023
NCT03455023Unknown不适用

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

Zhejiang Cancer Hospital1 个研究点 分布在 1 个国家目标入组 500 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
500
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 inpatients

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 inpatients.

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
否

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

  • •Current pregnancy or breastfeeding;
  • •Patients diagnosed with non-cancer pain;
  • •Patients treated with patient-controlled analgesia;
  • •Patients with pathological fracture, gastrointestinal obstruction, severe infection, non-opioid related intractable constipation;
  • •Patients with mental disorder;
  • •Creatinine clearance rate <15mL/min;
  • •ALT or AST ≥ 10 fold of upper limit of normal value

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 after discharge

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

次要结局

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

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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