The effects of nabiximols (Sativex®) on spasticity and non-motor symptoms in chronic spinal cord injury (SCI): a longitudinal prospective study.

IF 0.7 Q4 CLINICAL NEUROLOGY
Fernando Martins Braga, Sergiu Albu, Cecilia Mariño Fernández, Virginia Martínez Santana, Jesús Benito-Penalva, Joan Vidal Samsó
{"title":"The effects of nabiximols (Sativex®) on spasticity and non-motor symptoms in chronic spinal cord injury (SCI): a longitudinal prospective study.","authors":"Fernando Martins Braga, Sergiu Albu, Cecilia Mariño Fernández, Virginia Martínez Santana, Jesús Benito-Penalva, Joan Vidal Samsó","doi":"10.1038/s41394-025-00712-2","DOIUrl":null,"url":null,"abstract":"<p><strong>Study design: </strong>Observational, longitudinal, prospective study.</p><p><strong>Objectives: </strong>This study aimed to evaluate the effects of Nabiximols (Sativex®) on spasticity in chronic spinal cord injury (SCI) individuals refractory to conventional therapy. Secondary objectives included assessing its impact on functional independence, neuropathic pain, sleep quality, and depression.</p><p><strong>Setting: </strong>Institute Guttmann, a neurorehabilitation hospital in Badalona, Catalonia (Spain).</p><p><strong>Methods: </strong>Adult participants ( >18 years) with chronic SCI ( >6 months) and moderate to severe spasticity refractory to conventional treatments were recruited. All participants underwent baseline assessments and were followed up at one and two months after initiating treatment with nabiximols oromucosal spray, with individualised dose adjustments on a weekly basis. Assessed variables included spasticity, functional independence, neuropathic pain, sleep quality, depression, quality of life, and Patient Global Impression of Improvement (PGI-I).</p><p><strong>Results: </strong>Statistically significant improvements in spasticity were observed after one month (VAS decrease of 30%, p < 0.001; MAS decrease of 60%, p = 0.001) and two months (VAS decrease of 30%, p < 0.001; MAS decrease of 52%, p = 0.011) of treatment. A positive PGI-I was reported in 67% of participants. However, no significant changes were noted in spasms frequency, functional independence, neuropathic pain, or sleep quality. No significant differences in spasticity change or non-motor symptoms were found between participants with complete and incomplete SCI.</p><p><strong>Conclusions: </strong>Nabiximols may effectively reduce spasticity in individuals with SCI resistant to conventional therapies. Given the significant impact of spasticity associated with SCI, it could be considered a viable add-on therapy for this population.</p><p><strong>Trial registry: </strong>This clinical trial is registered in the EudraCT database under the identifier 2022-001777-31.</p><p><strong>Sponsorship: </strong>Almirall, S.A., Barcelona, Catalonia (Spain).</p>","PeriodicalId":22079,"journal":{"name":"Spinal Cord Series and Cases","volume":"11 1","pages":"19"},"PeriodicalIF":0.7000,"publicationDate":"2025-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12271395/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Spinal Cord Series and Cases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1038/s41394-025-00712-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Study design: Observational, longitudinal, prospective study.

Objectives: This study aimed to evaluate the effects of Nabiximols (Sativex®) on spasticity in chronic spinal cord injury (SCI) individuals refractory to conventional therapy. Secondary objectives included assessing its impact on functional independence, neuropathic pain, sleep quality, and depression.

Setting: Institute Guttmann, a neurorehabilitation hospital in Badalona, Catalonia (Spain).

Methods: Adult participants ( >18 years) with chronic SCI ( >6 months) and moderate to severe spasticity refractory to conventional treatments were recruited. All participants underwent baseline assessments and were followed up at one and two months after initiating treatment with nabiximols oromucosal spray, with individualised dose adjustments on a weekly basis. Assessed variables included spasticity, functional independence, neuropathic pain, sleep quality, depression, quality of life, and Patient Global Impression of Improvement (PGI-I).

Results: Statistically significant improvements in spasticity were observed after one month (VAS decrease of 30%, p < 0.001; MAS decrease of 60%, p = 0.001) and two months (VAS decrease of 30%, p < 0.001; MAS decrease of 52%, p = 0.011) of treatment. A positive PGI-I was reported in 67% of participants. However, no significant changes were noted in spasms frequency, functional independence, neuropathic pain, or sleep quality. No significant differences in spasticity change or non-motor symptoms were found between participants with complete and incomplete SCI.

Conclusions: Nabiximols may effectively reduce spasticity in individuals with SCI resistant to conventional therapies. Given the significant impact of spasticity associated with SCI, it could be considered a viable add-on therapy for this population.

Trial registry: This clinical trial is registered in the EudraCT database under the identifier 2022-001777-31.

Sponsorship: Almirall, S.A., Barcelona, Catalonia (Spain).

nabiximols (Sativex®)对慢性脊髓损伤(SCI)痉挛和非运动症状的影响:一项纵向前瞻性研究。
研究设计:观察性、纵向、前瞻性研究。目的:本研究旨在评估纳比昔醇(Sativex®)对传统治疗难治性慢性脊髓损伤(SCI)患者痉挛的影响。次要目的包括评估其对功能独立性、神经性疼痛、睡眠质量和抑郁的影响。环境:Guttmann研究所,西班牙加泰罗尼亚巴达洛纳的一家神经康复医院。方法:招募慢性SCI(>6个月)和常规治疗难治性中重度痉挛的成年参与者(>18岁)。所有参与者都接受了基线评估,并在开始使用纳比昔醇口腔喷雾剂治疗后的1个月和2个月进行了随访,并每周进行个体化剂量调整。评估变量包括痉挛、功能独立性、神经性疼痛、睡眠质量、抑郁、生活质量和患者总体改善印象(PGI-I)。结果:1个月后痉挛症状有统计学意义的改善(VAS下降30%)。结论:纳比ximols可有效降低对常规治疗有抵抗性的脊髓损伤患者的痉挛症状。考虑到与脊髓损伤相关的痉挛的显著影响,它可以被认为是这一人群可行的附加治疗。试验注册:该临床试验在EudraCT数据库中注册,标识符为2022-001777-31。赞助:Almirall, s.a.,巴塞罗那,加泰罗尼亚(西班牙)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Spinal Cord Series and Cases
Spinal Cord Series and Cases Medicine-Neurology (clinical)
CiteScore
2.20
自引率
8.30%
发文量
92
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信