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临床试验/NCT03245658
NCT03245658撤回2 期

The Effect of Medical Cannabis Inpatients With Palliative Pancreatic Cancer

Jens Rikardt Andersen1 个研究点 分布在 1 个国家开始时间: 2017年10月6日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
撤回
发起方
试验地点
1
主要终点
Energy and protein intake

研究概览

简要总结

Cannabinoids are known to increase appetite, but THC components have psychogenic properties too. CBD is the main component in the plant, and have only minimal psychogenic effects. The aim was to test the appetite stimulating effects of CBD in patients with pancreatic cancer in palliative treatment.

详细描述

Randomization of consecutive patients who wanted to participate to a daily dose of CBD or not as a supplement to the standard treatment.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
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

  • Adult, palliative pancreatic cancer diagnosis, weight loss > 5%, understand and read Danish.

排除标准

  • Regular use of cannabis, psychiatric disorders, alcohol abuse, life expectancy < 6 months

研究组 & 干预措施

THC and CBD Mixture

Experimental

32 patients with palliative pancreatic cancer, intervention with oral drops of THC, 25mg/ml and CBD 50mg/ml, daily administered for 4 weeks

干预措施: THC and CBD Mixture (Drug)

结局指标

主要结局

Energy and protein intake

时间窗: The outcome measure will be assessed at day 0 and at week 4

Dietary history (% of estimated needs - NRS 2002)

次要结局

  • Lean body mass(The outcome measure will be assessed at day 0 and at week 4)
  • Appetite 1(The outcome measure will be assessed at day 0 and at week 4)
  • Appetite 2(The outcome measure will be assessed at day 0 and at week 4)
  • Appetite 3(The outcome measure will be assessed at day 0 and at week 4)
  • Appetite 4(The outcome measure will be assessed at day 0 and at week 4)
  • Quality of life 1(The outcome measure will be assessed at day 0 and at week 4)
  • Quality of life 2(The outcome measure will be assessed at day 0 and at week 4)
  • Quality of life 3(The outcome measure will be assessed at day 0 and at week 4)
  • Pain 1(The outcome measure will be assessed at day 0 and at week 4)
  • Pain 2(The outcome measure will be assessed at day 0 and at week 4)
  • Pain 3(The outcome measure will be assessed at day 0 and at week 4)
  • Mortality (8 weeks)(8 weeks)

研究者

发起方
Jens Rikardt Andersen
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jens Rikardt Andersen

Associate Professor

University of Copenhagen

研究点 (1)

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