EUCTR2007-000805-32-GB进行中（未招募）1 期
AN INVESTIGATION INTO THE ROLE OF PARACETAMOL (ACETAMINOPHEN) AT STEP 3 OF THE WHO ANALGESIC LADDER
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中（未招募）
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
入选标准
- •1.Clinical diagnosis of cancer.
- •2.Age =18yr.
- •3.Taking regular opioids for moderate to severe pain (i.e. 4hrly normal release opioid; 12hourly modified release opioid; or a transdermal patch - step 3 of the WHO analgesic ladder) for the preceding 7 days.
- •4.Taking = 2g / day paracetamol for the preceding 7 days.
- •5.Average pain score for the preceding 24hrs =4 on a 0-10 numerical rating scale (NRS).
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •1.Unwilling to stop paracetamol
- •2.No diagnosis of malignant disease.
- •3.Age <18yr.
- •4.Prognosis <2weeks.
- •5.Radiotherapy treatment in the preceding 4 weeks.
- •6.New anti-cancer treatment in the preceding 4 weeks.
- •7.Average pain score for the preceding 24hrs =5 on NRS.
- •8.Significant cognitive impairment, i.e. unable to complete pain questionnaire.
研究者
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