大麻二酚与布洛芬缓解女性原发性痛经疼痛的疗效:II期非劣效性试验

Haneesha Mohan
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摘要

简介:疼痛是原发性痛经(PDM)女性的主要症状,对她们的生活质量产生了无情的负面影响。患有PDM的女性子宫内膜液中前列腺素水平较高,这与疼痛程度有关。PDM相关疼痛的标准治疗开始于非甾体抗炎药(NSAIDs),阻断前列腺素触发酶。尽管非甾体抗炎药是一种可行的选择,但它们也有显著的副作用风险。大约20%到25%的患者会对非甾体抗炎药产生难治性疼痛,并寻求替代疗法。大麻二酚(CBD)是一种耐受性良好的潜在治疗多种慢性疾病,包括疼痛,并通过阻断前列腺素触发酶起作用,类似于非甾体抗炎药。CBD的安全性是公认的,具有通过中枢和外周机制起作用的优势。迄今为止,还没有单独评估CBD治疗痛经的试验。目的:通过总疼痛缓解(TOTPAR)量表评估CBD与布洛芬在减轻急性经期疼痛方面的效果。设计:随机(随机分组大小)、三盲、多中心、平行组、非劣效性临床试验。参与者:年龄18 - 40岁,月经周期正常(21 - 35天),视觉模拟评分(VAS)评分≥5的PDM患者。学术编辑:Felipe Fregni同行评审:Natalia Suarez;Giovani淀粉;Magali Andrea Pestana;路易斯·莫拉莱斯·奥赫达。版权所有:©2022作者所有。知识共享署名(CC BY)许可(https://creativecommons.org/licenses/by/4.0/)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy of Cannabidiol Versus Ibuprofen in the Relief of Menstrual Pain in Females Living with Primary Dysmenorrhea A phase II, Non-Inferiority trial
Introduction: Pain is the cardinal symptom in women living with primary dysmenorrhea (PDM), resulting in a relentless negative effect on their quality of life. Women with PDM have higher levels of prostaglandin in their endometrial fluid, which correlates with the degree of pain. The standard of care treatment for pain associated with PDM starts with nonsteroidal anti-inflammatory drugs (NSAIDs) that block prostaglandin-triggering enzymes. Although NSAIDs are a feasible option, they are also associated with a significant risk of side effects. Around 20 to 25% of patients will experience pain refractory to NSAIDs and seek alternative therapies. Cannabidiol (CBD) is a well-tolerated potential therapy for several chronic diseases, including pain, and acts by blocking prostaglandin-triggering enzymes, similar to NSAIDs. The safety of CBD is well established, with the advantage of acting via central and peripheral mechanisms. To date, no previous trials assessing CBD alone for dysmenorrhea have been conducted. Objective: To evaluate the effect of CBD alone in reducing acute menstrual pain compared to ibuprofen, as assessed by the total pain relief (TOTPAR) scale. Design: Randomized (with random block sizes), triple-blinded, multicenter, parallel-group, non-inferiority clinical trial. Participants: PDM patients aged 18 to 40 years, with regular menstrual cycles (ranging from 21 to 35 days) and a visual analog scale (VAS) score of ≥ 5. Academic Editor: Felipe Fregni Peer-reviewers: Natalia Suarez; Giovani Farina; Magali Andrea Pestana; Luis Morales Ojeda. Copyright: © 2022 by the authors. Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
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