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多中心、青少年慢性头痛大麻素草药提取物中富含大麻二酚的耐受性研究:CAN-CHA 方案。

A multi-centre, tolerability study of a cannabidiol-enriched Cannabis Herbal Extract for chronic headaches in adolescents: The CAN-CHA protocol.

机构信息

Department of Pharmacology & Therapeutics, Max Rady College of Medicine, University of Manitoba, Winnipeg, Manitoba, Canada.

North Toronto Neurology, Toronto, Ontario, Canada.

出版信息

PLoS One. 2024 Sep 20;19(9):e0290185. doi: 10.1371/journal.pone.0290185. eCollection 2024.

Abstract

INTRODUCTION

Cannabis products have been used in the management of headaches in adults and may play a role in pediatric chronic pain. Canadian pediatricians report increasing use of cannabis for the management of chronic headaches, despite no well-controlled studies to inform its dosing, safety, and effectiveness. The aim of our clinical trial is to determine the dosing and safety of a Cannabidiol (CBD)-enriched Cannabis Herbal Extract (CHE) for the treatment of chronic headaches in adolescents.

METHODS AND ANALYSIS

Youth, parents, and an expert steering committee co-designed this tolerability study. Twenty adolescents (aged 14 to 17 years), with a chronic migraine diagnosis for more than 6 months that has not responded to other therapies will be enrolled into an open label, dose escalation study across three Canadian sites. Study participants will receive escalating doses of a CBD-enriched CHE (MPL-001 with a THC:CBD of 1:25), starting at 0.2-0.4 mg/kg of CBD per day and escalating monthly up to 0.8-1.0 mg/kg of CBD per day. The primary objective of this study is to determine the safety and tolerability of CBD-enriched CHE in adolescents with chronic migraine. Secondary objectives of this study will inform the development of subsequent randomized controlled trials and include investigating the relationship between the dose escalation and change in the frequency of headache, impact and intensity of pain, changes in sleep, mood, function, and quality of life. Exploratory outcomes include investigating steady-state trough plasma levels of bioactive cannabinoids and investigating how pharmacogenetic profiles affect cannabinoid metabolism among adolescents receiving CBD-enriched CHE.

DISCUSSION

This protocol was co-designed with youth and describes a tolerability clinical trial of CBD-enriched CHE in adolescents with chronic headaches that have not responded to conventional therapies. This study is the first clinical trial on cannabis products in adolescents with chronic headaches and will inform the development of future comparative effectiveness clinical trials.

TRIAL REGISTRATION

CAN-CHA trial is registered with ClinicalTrials.gov with a number of register NCT05337033.

摘要

简介

大麻制品已被用于成人头痛的治疗,并且可能在儿童慢性疼痛中发挥作用。尽管没有良好对照的研究来告知其剂量、安全性和有效性,但加拿大儿科医生报告说,大麻在管理慢性头痛方面的使用越来越多。我们的临床试验旨在确定大麻素(CBD)丰富的大麻草药提取物(CHE)治疗青少年慢性头痛的剂量和安全性。

方法和分析

青年、家长和一个专家指导委员会共同设计了这项耐受性研究。将招募 20 名患有慢性偏头痛(诊断时间超过 6 个月且对其他治疗无反应)的青少年(年龄在 14 至 17 岁之间)进入加拿大三个地点的开放标签、剂量递增研究。研究参与者将接受递增剂量的 CBD 丰富 CHE(MPL-001,THC:CBD 为 1:25),起始剂量为每天 0.2-0.4 毫克/公斤 CBD,每月递增至每天 0.8-1.0 毫克/公斤 CBD。本研究的主要目的是确定 CBD 丰富 CHE 在患有慢性偏头痛的青少年中的安全性和耐受性。本研究的次要目标将为随后的随机对照试验提供信息,包括调查剂量递增与头痛频率变化、疼痛影响和强度、睡眠、情绪、功能和生活质量变化之间的关系。探索性结果包括调查生物活性大麻素的稳态谷血浆水平,以及调查接受 CBD 丰富 CHE 的青少年中药物遗传学特征如何影响大麻素代谢。

讨论

该方案是与年轻人共同设计的,描述了一项 CBD 丰富 CHE 在对常规治疗无反应的慢性头痛青少年中的耐受性临床试验。这是第一项关于慢性头痛青少年中大麻产品的临床试验,将为未来的比较有效性临床试验提供信息。

试验注册

CAN-CHA 试验在 ClinicalTrials.gov 上注册,注册号为 NCT05337033。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4163/11414974/86c3155d8c66/pone.0290185.g001.jpg

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