裸盖菇素辅助治疗成人纤维肌痛的初步安全性和有效性:一项开放标签的试点临床试验

IF 2.5 Q2 CLINICAL NEUROLOGY
Frontiers in pain research (Lausanne, Switzerland) Pub Date : 2025-03-18 eCollection Date: 2025-01-01 DOI:10.3389/fpain.2025.1527783
Jacob S Aday, Jenna McAfee, Deirdre A Conroy, Avinash Hosanagar, Vijay Tarnal, Cody Weston, Katherine Scott, Dana Horowitz, Jamarie Geller, Steven E Harte, Niloufar Pouyan, Nicolas G Glynos, Anne K Baker, Jeffrey Guss, Alan K Davis, Helen J Burgess, George A Mashour, Daniel J Clauw, Kevin F Boehnke
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引用次数: 0

摘要

纤维肌痛(FM)是一种典型的伤害性疼痛,其特征是广泛的疼痛和认知、情绪和睡眠问题。目前,可有效治疗FM症状的治疗方案有限。裸盖菇素辅助治疗(PAT)是一种新兴的联合药物治疗干预,但迄今为止尚无研究调查PAT治疗FM。方法:在这里,我们报告了一项开放标签,PAT治疗FM的临床试验结果(N = 5)。与心理治疗(两次预备,四次整合)相结合,参与者接受两剂量的口服裸盖菇素(15毫克和25毫克),间隔两周。结果:关于安全性(主要结局),在给药期间血压或心率短暂升高,在治疗结束时恢复正常,无严重不良事件。五分之四的参与者在服药后报告了短暂性头痛。与基线相比,受试者报告在第二次裸盖菇素剂量一个月后(以Cohen’s d报告),以下次要结果有临床意义的改善:疼痛严重程度[d = -2.1, 95% CI(-3.7至-0.49)],疼痛干扰[d = -1.8, 95% CI(-3.27至-0.24)],睡眠障碍[d = -2.5, 95% CI(-4.21至-0.75)]。使用患者整体印象改变,一个参与者报告他们的症状“非常改善”,两个报告“非常改善”,两个报告“最低限度改善”。我们提前停止了招募,因为考虑到药物临床试验的普遍性和FDA指南在数据收集方面的变化。讨论:这项小型开放标签试验初步支持了FM患者对PAT的良好耐受,为更大规模的随机对照试验奠定了基础。临床试验注册:ClinicalTrials.gov,识别码,(NCT05128162)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preliminary safety and effectiveness of psilocybin-assisted therapy in adults with fibromyalgia: an open-label pilot clinical trial.

Introduction: Fibromyalgia (FM) is the prototypical nociplastic pain condition, characterized by widespread pain and issues with cognition, mood, and sleep. Currently, there are limited treatment options available that effectively treat FM symptoms. Psilocybin-assisted therapy (PAT) is an emerging combined drug-therapy intervention, but no studies to-date have investigated PAT for FM.

Methods: Here, we report findings from an open-label, pilot clinical trial of PAT for FM (N = 5). In conjunction with psychotherapy (two preparatory, four integration sessions), participants received two doses of oral psilocybin (15 mg and 25 mg) delivered two weeks apart.

Results: Regarding safety (primary outcome), there were transient elevations of blood pressure or heart rate during dosing which normalized by the end of treatment, with no serious adverse events. Four of five participants reported transient headaches following dosing. Compared to baseline, participants reported clinically meaningful improvements in the following secondary outcomes one month following their second psilocybin dose (reported as Cohen's d): pain severity [d = -2.1, 95% CI(-3.7 to -0.49)], pain interference [d = -1.8, 95% CI (-3.27 to -0.24)], and sleep disturbance [d = -2.5, 95% CI (-4.21 to -0.75)]. Using the Patient Global Impression of Change, one participant reported their symptoms "very much improved," two reported "much improved," and two reported "minimally improved." We stopped recruitment early because of concerns about generalizability and changes in FDA guidance for psychedelic clinical trials that occurred data collection.

Discussion: This small open-label trial preliminarily supports that PAT is well-tolerated by people with FM, establishing a basis for larger randomized controlled trials.

Clinical trial registration: ClinicalTrials.gov, identifier, (NCT05128162).

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