The Lambert Initiative for Cannabinoid Therapeutics, The University of Sydney, Sydney, New South Wales, Australia.
Sydney Pharmacy School, The University of Sydney, Sydney, New South Wales, Australia.
Sci Rep. 2024 May 23;14(1):11792. doi: 10.1038/s41598-024-62428-x.
Hand osteoarthritis (OA) is an irreversible degenerative condition causing chronic pain and impaired functionality. Existing treatment options are often inadequate. Cannabidiol (CBD) has demonstrated analgesic and anti-inflammatory effects in preclinical models of arthritis. In this open-label feasibility trial, participants with symptomatically active hand OA applied a novel transdermal CBD gel (4% w/w) three times a day for four weeks to their most painful hand. Changes in daily self-reported pain scores were measured on a 0-10 Numeric Pain Rating Scale (NPRS). Hand functionality was determined via daily grip strength measures using a Bluetooth equipped squeeze ball and self-report questionnaire. Quality of life (QoL) ratings around sleep, anxiety, stiffness and fatigue were also measured. All self-report measures and grip strength data were gathered via smartphone application. Urinalysis was conducted at trial end to determine systemic absorption of CBD. Eighteen participants were consented and 15 completed the trial. Pain ratings were significantly reduced over time from pre-treatment baseline including current pain (- 1.91 ± 0.35, p < 0.0001), average pain (- 1.92 ± 0.35, p < 0.0001) and maximum pain (- 1.97 ± 0.34, p < 0.0001) (data represent mean reduction on a 0-10 NPRS scale ± standard error of the mean (SEM)). A significant increase in grip strength in the treated hand (p < 0.0001) was observed although self-reported functionality did not improve. There were significant (p < 0.005) improvements in three QoL measures: fatigue, stiffness and anxiety. CBD and its metabolites were detected at low concentrations in all urine samples. Measured reductions in pain and increases in grip strength seen during treatment reverted back towards baseline during the washout phase. In summary, pain, grip strength and QoL measures, using smartphone technology, was shown to improve over time following transdermal CBD application suggesting feasibility of this intervention in relieving osteoarthritic hand pain. Proof of efficacy, however, requires further confirmation in a placebo-controlled randomised trial.Trial registration: ANZCTR public trials registry (ACTRN12621001512819, 05/11/2021).
手部骨关节炎(OA)是一种不可逆转的退行性疾病,会导致慢性疼痛和功能受损。现有的治疗选择往往不够充分。大麻二酚(CBD)在关节炎的临床前模型中显示出了镇痛和抗炎作用。在这项开放性、可行性试验中,患有症状性活动性手部 OA 的参与者每天三次在其最疼痛的手上涂抹一种新型的透皮 CBD 凝胶(4%w/w),持续四周。使用配备蓝牙的挤压球和自我报告问卷,每天测量自我报告的疼痛评分变化。通过智能手机应用程序收集手部功能的日常握力测量数据和自我报告问卷。还测量了睡眠、焦虑、僵硬和疲劳方面的生活质量(QoL)评分。所有自我报告的测量和握力数据都是通过智能手机应用程序收集的。试验结束时进行尿液分析以确定 CBD 的全身吸收情况。18 名参与者同意参加试验,其中 15 名完成了试验。疼痛评分随着时间的推移从治疗前基线显著降低,包括当前疼痛(-1.91±0.35,p<0.0001)、平均疼痛(-1.92±0.35,p<0.0001)和最大疼痛(-1.97±0.34,p<0.0001)(数据表示 0-10 NPRS 量表上的平均降低值±均值的标准误差(SEM))。虽然自我报告的功能没有改善,但在治疗手的握力显著增加(p<0.0001)。在三个 QoL 指标方面观察到显著(p<0.005)改善:疲劳、僵硬和焦虑。所有尿液样本中均检测到 CBD 及其代谢物的低浓度。治疗期间观察到的疼痛减轻和握力增加,在洗脱期又恢复到基线水平。总之,使用智能手机技术,随着时间的推移,在接受透皮 CBD 治疗后,疼痛、握力和 QoL 测量均有所改善,这表明这种干预措施缓解手部骨关节炎疼痛是可行的。然而,需要在安慰剂对照随机试验中进一步证实其疗效。试验注册:澳大利亚新西兰临床试验注册中心公共试验注册(ACTRN12621001512819,2021 年 11 月 5 日)。