跳至主要内容
临床试验/CTIS2024-513593-22-00
CTIS2024-513593-22-00进行中(未招募)1 期

BONG: Reducing severe Breathlessness with Dronabinol in the severe and very severe chronic obstructive pulmonary disease patient group

illebaelt Hospital0 个研究点目标入组 30 人开始时间: 2024年4月22日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 65+(—)
性别
All

入选标准

  • Refractory dyspnea despite optimal treatment, COPD (GOLD 3,4), Breathlessness corresponding to mMRC score = 3, Informed written consent, Age = 18 years, Cognitive relevant, of legal age, Understands and speaks Danish, For fertile women defined by amenorrhea for less than 12 months: negative HCG before entry into the trial, For fertile and sexually active subjects: use of safe contraception during medication intake and 4 weeks after: intrauterine device (IUD) or hormonal contraception (oral contraceptive pill, implant, transdermal patch, vaginal ring or depot injection).

排除标准

  • Ongoing infection or exacerbation of COPD within the last month (30 days), Regular treatment with THC or CBD within 1 month (30 days), Life expectancy less than 3 months (90 days), Treatment with medicines that, according to the summary of product characteristics, are strong inhibitors or inducers of CYP3A4, CYP2C9 or CYP2C19, History of or current evidence of significant medical or psychiatric disorder that is considered by the investigator to put the subject at greater risk of experiencing an adverse event, Current or past substance abuse where the investigator finds it too risky for the subject to be included in the study

研究者

发起方
illebaelt Hospital

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