[Efficacy and safety of Cytoflavin in the treatment of diabetic polyneuropathy: results of a multicenter, double-blind, placebo-controlled, randomized CYLINDER study].

I A Strokov, Yu A Trakhtenberg, A L Kovalenko
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引用次数: 1

Abstract

Objective: The purpose of the present double-blind, placebo-controlled, randomized clinical trial was to evaluate the efficacy and safety of Cytoflavin in patients with diabetic polyneuropathy (DPN).

Material and methods: Investigational therapy was administered in two steps: intravenous infusions of experimental drug/placebo for 10 days followed by oral administration for 75 days. In 10 clinical centers, 216 patients aged 45-74 years with a diagnosis of type 2 diabetes mellitus, symptomatic distal sensorimotor DPN, confirmed no earlier than 1 year before screening, on stable therapy (no change of drugs and doses) by oral hypoglycemic drugs, intermediate-acting, long-acting or extra-long-acting insulin, and/or GLP-1 receptor agonists.

Results: By the end of treatment, the change of the Total Symptom Score (TSS) in the experimental group was -2.65 points, in the placebo group -1.73 points (p<0.001). Improvement of symptoms in the experimental group was achieved regardless of the degree of compensation for type 2 diabetes (both in those with Hb1Ac <8.0% and in those with Hb1Ac ≥8.0%), but demonstrated better results in patients with less severe baseline symptoms (TSS <7.5). Improvement in the components of the TSS scale «paresthesia» and «numbness» occurred as early as on day 11 of therapy; by the end of treatment, a significant decrease in the «burning» component was also demonstrated. The experimental drug had a positive safety profile.

Conclusion: Cytoflavin, intravenous solution and enteric-coated tablets (SPTF Polysan Ltd.) is indicated for the symptomatic treatment of DPN.

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[细胞黄素治疗糖尿病多发神经病变的疗效和安全性:一项多中心、双盲、安慰剂对照、随机圆柱体研究的结果]。
目的:本双盲、安慰剂对照、随机临床试验的目的是评价细胞黄素治疗糖尿病多发神经病变(DPN)的疗效和安全性。材料和方法:研究治疗分两步进行:静脉滴注实验药物/安慰剂10天,口服75天。在10个临床中心,216例年龄45-74岁,诊断为2型糖尿病,症状性远端感觉运动DPN的患者,在筛查前不早于1年确诊,口服降糖药、中效、长效或超长效胰岛素和/或GLP-1受体激动剂稳定治疗(药物和剂量不变)。结果:治疗结束时,试验组总症状评分(TSS)变化为-2.65分,安慰剂组总症状评分变化为-1.73分(p)。结论:细胞黄素静脉滴注肠溶片(SPTF多糖有限公司)适用于DPN的对症治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova Medicine-Psychiatry and Mental Health
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