首页> 外文期刊>Trials >Oral medicinal cannabinoids to relieve symptom burden in the palliative care of patients with advanced cancer: a double-blind, placebo-controlled, randomised clinical trial of efficacy and safety of 1:1 delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD)
【24h】

Oral medicinal cannabinoids to relieve symptom burden in the palliative care of patients with advanced cancer: a double-blind, placebo-controlled, randomised clinical trial of efficacy and safety of 1:1 delta-9-tetrahydrocannabinol (THC) and cannabidiol (CBD)

机译:口腔药用大麻素可缓解癌症患者姑息治疗的症状负担:一种双盲,安慰剂控制,随机临床试验,疗效和安全性为1:1δ-9-四氢胺(THC)和大麻(CBD)

获取原文
           

摘要

Despite improvements in medical care, patients with advanced cancer still experience substantial symptom distress. There is increasing interest in the use of medicinal cannabinoids but little high-quality evidence to guide clinicians. This study aims to define the role of a 1:1 delta-9-tetrahydrocannabinol/cannabidiol (THC/CBD) cannabinoid preparation in the management of symptom burden in patients with advanced cancer undergoing standard palliative care. One hundred fifty participants will be recruited from five sites within the Queensland Palliative Care Research Group (QPCRG) and randomly assigned to an active treatment or placebo group. This study is a pragmatic multicentre, randomised, placebo-controlled, two-arm trial of escalating doses of an oral 1:1 THC/CBD cannabinoid preparation. It will compare efficacy and safety outcomes of a titrated dose (10?mg/10?mg/mL oral solution formulation, dose range 2.5?mg/2.5?mg–30?mg/30?mg/day) against placebo. There is a 2-week patient-determined titration phase, using escalating doses of 1:1 THC/CBD or placebo, to reach a dose that achieves symptom relief with tolerable side effects. This is then followed by a further 2-week assessment period on the stable dose determined in collaboration with clinicians. The primary objective is to assess the effect of escalating doses of a 1:1 THC/CBD cannabinoid preparation against placebo on change in total symptom score, with secondary objectives including establishing a patient-determined effective dose, the change in total physical and emotional sores, global impression of change, anxiety and depression, opioid use, quality of life and adverse effects. This will be the first placebo-controlled clinical trial to rigorously evaluate the efficacy, safety and acceptability of 1:1 THC/CBD for symptom relief in advanced cancer patients. This study will allow the medical community to have some evidence to present to patients wishing to access cannabis for their symptoms caused by advanced malignancy.
机译:尽管医疗保健改善,患有先进癌症的患者仍然体验着大量症状困扰。在使用药物大麻素的情况下,越来越感兴趣,但是指导临床医生的高质量证据。本研究旨在定义1:1δ-9-四氢甘油醛/大麻(THC / CBD)大麻素制剂在患有先进癌症的患者患者的症状负担管理中的作用。将从昆士兰州姑藏姑息治疗研究组(QPCRG)中的五个站点招募了一百五十名参与者,并随机分配给活跃治疗或安慰剂组。本研究是一种务实的多期多期,随机,安慰剂控制的双臂试验,其升级口腔1:1 THC / CBD大麻制剂的剂量。它将比较滴定剂量的功效和安全结果(10×mg / 10×mg / ml口服溶液制剂,剂量范围为2.5〜mg / 2.5?mg-30?mg / 30?mg / day),适用于安慰剂。使用升级剂量为1:1 THC / CBD或安慰剂,达到2周的患者确定的滴定阶段,以达到具有可容忍副作用的症状浮雕的剂量。然后在与临床医生协作确定的稳定剂量上进行其它2周评估期。主要目的是评估升级1:1 Thc / CBD大麻素对症状评分变化的升级剂量的效果,其中次要目标包括建立患者确定的有效剂量,整个身体和情绪疮的变化,全球对变革,焦虑和抑郁,阿片类药物使用,生活质量和不良影响的印象。这将是第一个安慰剂对照的临床试验,以严格评估1:1 THC / CBD的疗效,安全性和可接受性,用于晚期癌症患者的症状缓解。本研究将允许医学界有一些证据表明希望能够进入大麻症状引起的恶性肿瘤症状的患者。

著录项

相似文献

  • 外文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号