首页> 外文期刊>Evidence-based complementary and alternative medicine: eCAM >The homeopathic preparation Nervoheel N can offer an alternative to lorazepam therapy for mild nervous disorders.
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The homeopathic preparation Nervoheel N can offer an alternative to lorazepam therapy for mild nervous disorders.

机译:顺势疗法制剂Nervoheel N可为劳拉西m治疗提供轻度神经疾病的替代疗法。

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摘要

In an open-label, prospective non-randomized cohort study, we compared the effectiveness and tolerability profiles of the homeopathic remedy Nervoheel N with those of the benzodiazepine, lorazepam, in 248 patients with insomnia, distress, anxieties, restlessness or burnout and similar nervous conditions ('mild nervous disorders'). Patients were treated with Nervoheel N or lorazepam at the recommended doses for a maximum of 4 weeks. Dose variations were allowed if in the patient's best interest. Treatment effects were evaluated by the practitioner in a dialogue with the patient at the start of treatment, after 2 weeks and after maximally 4 weeks of treatment. Tolerability data were recorded as adverse events. At baseline, lorazepam patients were on average slightly older and there was a somewhat greater percentage of men in this group than in the Nervoheel group. Both treatment groups reported significant symptomatic improvements of similar magnitude during the course of the study. The sum of symptom scores improved by 4.4 points with Nervoheel N and by 4.2 points with lorazepam. The differences between the treatment groups were not significant. All differences between treatments were within 10% of the maximum score ranges, demonstrating non-inferiority of Nervoheel N. Both treatments were well tolerated, with few adverse events and very good self-assessed tolerability ratings by the patients. Thus, in patients who opt for a homeopathic treatment regimen for the short-term relief of mild nervous disorders, the effects of Nervoheel N are non-inferior to those of lorazepam.
机译:在一项开放性,前瞻性,非随机队列研究中,我们比较了顺势疗法药物Nervoheel N与苯二氮卓,劳拉西m的疗效和耐受性特征,对248名失眠,困扰,焦虑,不安或倦怠和类似神经症的患者进行了比较状况(“轻度神经障碍”)。用推荐剂量的Nervoheel N或劳拉西m治疗患者,最长4周。如果符合患者的最大利益,则允许剂量变化。在治疗开始时,治疗后2周和最多治疗4周后,由执业医师与患者进行对话以评估治疗效果。耐受性数据记录为不良事件。基线时,劳拉西m患者的平均年龄稍大,并且该组的男性百分比比Nervoheel组的男性略高。在研究过程中,两个治疗组均报告了相似程度的明显症状改善。 Nervoheel N的症状得分总和提高了,劳拉西m的症状得分提高了4.2分。治疗组之间的差异不显着。治疗之间的所有差异均在最大得分范围的10%之内,这表明Nervoheel N不劣。两种治疗均耐受良好,几乎没有不良事件,并且患者的自我评估耐受性评分非常好。因此,在为短期缓解轻度神经障碍而选择顺势疗法的患者中,Nervoheel N的作用不逊于劳拉西m。

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