口服大麻二酚和四氢大麻酚治疗特发性震颤的双盲、随机、安慰剂对照交叉研究。

IF 2.5 Q2 CLINICAL NEUROLOGY
Tremor and Other Hyperkinetic Movements Pub Date : 2025-04-14 eCollection Date: 2025-01-01 DOI:10.5334/tohm.1005
Katherine Longardner, Qian Shen, Francisco X Castellanos, Bin Tang, Rhea Gandhi, Brenton A Wright, Jeremiah D Momper, Fatta B Nahab
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引用次数: 0

摘要

背景:特发性震颤(ET)以致残性震颤为特征。目前还没有专门用于对症治疗的药物。坊间报道说大麻能改善震颤,但没有证据支持这些说法。我们在ET患者中进行了一项Ib/II期双盲、安慰剂对照、交叉试验,以研究Tilray TN-CT120 LM的耐受性、安全性和有效性,Tilray TN-CT120 LM是一种口服药物级制剂,含有四氢大麻酚(THC) 5毫克和大麻二酚(CBD) 100毫克。我们的目的是确定短期四氢大麻酚/CBD暴露是否改善震颤幅度和耐受性。方法:ET患者随机(1:1)接受TN-CT120 LM或安慰剂治疗。根据耐受性,每2-3天尝试一次剂量滴定,最多每日3粒。在返回完成评估之前,参与者保持最高耐受剂量两周。在完成第一组后,参与者滴定了药物,经历了三周的洗脱期,然后返回使用替代化合物进行相同的程序。主要终点是使用数字螺旋评估从基线开始的震颤幅度变化。次要终点探讨安全性和耐受性。结果:在筛选的13名参与者中,有7名符合条件并入组。其中5人完成了所有的访问;一名患者在发生严重不良事件后退出治疗,另一名患者无法耐受最低剂量。对6名参与者进行的意向治疗分析未显示对主要终点或次要终点的显著影响。结论:该试点试验未发现THC/CBD对ET有效的任何信号。虽然由于样本量小而处于初步阶段,但我们的数据不支持大麻素对ET有效的轶事报道。这项双盲、随机、安慰剂对照的疗效和耐受性先导试验没有发现口服大麻二酚和四氢大麻酚在使用数字结果测量或临床评定量表降低特发性震颤振幅方面的任何疗效信号。大多数(七分之五)参与者对口服大麻素耐受良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Double-Blind, Randomized, Placebo-Controlled, Crossover Study of Oral Cannabidiol and Tetrahydrocannabinol for Essential Tremor.

Background: Essential tremor (ET) is characterized by often disabling action tremors. No pharmacological agent has been developed specifically for symptomatic treatment. Anecdotal reports describe tremor improvement with cannabis, but no evidence exists to support these claims. We conducted a phase Ib/II double-blind, placebo-controlled, crossover pilot trial in participants with ET to investigate tolerability, safety, and efficacy of Tilray TN-CT120 LM, an oral pharmaceutical-grade formulation containing tetrahydrocannabinol (THC) 5 mg and cannabidiol (CBD) 100 mg. Our objectives were to determine if short-term THC/CBD exposure improved tremor amplitude and was tolerated.

Methods: Participants with ET were randomized (1:1) to receive either TN-CT120 LM or placebo. Dose titration, driven by tolerability, was attempted every 2-3 days to three capsules daily maximum. Participants remained on the highest tolerated dose for two weeks before returning to complete assessments. After completing the first arm, participants titrated off the agent, underwent a three-week washout, and then returned for the same procedures with the alternate compound. The primary endpoint was tremor amplitude change from baseline using digital spiral assessment. Secondary endpoints explored safety and tolerability.

Results: Among thirteen participants screened, seven were eligible and enrolled. Five completed all visits; one withdrew following a serious adverse event, and another did not tolerate the lowest dose. Intent-to-treat analyses performed for six participants did not reveal significant effects on primary or secondary endpoints.

Conclusions: This pilot trial did not detect any signals of efficacy of THC/CBD in ET. Although preliminary due to the small sample size, our data do not support anecdotal reports of cannabinoid effectiveness for ET.

Highlights: This double-blind, randomized, placebo-controlled efficacy and tolerability pilot trial did not detect any signals of efficacy of oral cannabidiol and tetrahydrocannabinol in reducing essential tremor amplitude using either digital outcome measures or clinical rating scales. The oral cannabinoids were well-tolerated by most (five out of seven) participants.

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来源期刊
CiteScore
4.00
自引率
4.50%
发文量
31
审稿时长
6 weeks
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