首页> 外文期刊>European journal of gastroenterology and hepatology >Extended analysis of a double-blind, placebo-controlled, 15-week study with otilonium bromide in irritable bowel syndrome.
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Extended analysis of a double-blind, placebo-controlled, 15-week study with otilonium bromide in irritable bowel syndrome.

机译:一项关于双盲,安慰剂对照,为期15周的溴化乙锭治疗肠易激综合征的研究的扩展分析。

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BACKGROUND/OBJECTIVE: In order to follow the most recent developments and recommendations in trial methodology for drug evaluation in patients with irritable bowel syndrome, we performed an extended analysis of a large clinical trial from a previously published study of otilonium bromide, using an assessment that integrates the key symptoms of irritable bowel syndrome. MATERIALS AND METHODS: A large-scale clinical trial with a double-blind, placebo-controlled, parallel-group study design was conducted in 378 patients, treated for 15 weeks with the recommended standard dose of 40 mg otilonium bromide or placebo three times daily. The study was based on the collection of 12 single efficacy endpoints. The new efficacy assessment was based on the data reported by the patients. Rather than demonstrating score differences between the treatment groups of the study, we carried out an assessment that integrates the most frequent symptoms reported (pain frequency and intensity, presence of meteorism and distension) by the patient. RESULTS: The rate of response to treatment within 2-4 months (the primary efficacy outcome measure) was significantly higher in the otilonium bromide group (36.9%) than in the placebo group (22.5%; P = 0.007). In each month of treatment, the rate of monthly response was higher in the otilonium bromide group as compared to the placebo group (P < 0.05). The total monthly and weekly responses to the single endpoints (intensity and frequency of pain and discomfort, meteorism/abdominal distension, severity of diarrhoea or constipation and mucus in the stool) were significantly more frequent in the group treated with otilonium bromide than in the placebo-treated group, with differences ranging from 10% to 20%. The subgroup analysis of the intestinal habits endpoint indicates that patients with diarrhoea have an additional benefit. CONCLUSION: The present re-evaluation of a previously published study confirms that otilonium bromide is more effective than placebo for the treatment of irritable bowel syndrome, being very efficient in relieving pain and discomfort.
机译:背景/目的:为了追踪肠易激综合征患者药物评估试验方法的最新发展和建议,我们对先前发表的溴化奥替铵的一项研究进行了一项大型临床试验的扩展分析,整合了肠易激综合症的关键症状。材料与方法:一项对378名患者进行了一项双盲,安慰剂对照,平行组研究设计的大规模临床试验,每天推荐3次,推荐剂量为40 mg溴化乙锭或安慰剂,治疗15周。该研究基于12个单一功效终点的收集。新的疗效评估基于患者报告的数据。我们没有显示研究治疗组之间的评分差异,而是进行了评估,该评估整合了患者报告的最常见症状(疼痛频率和强度,流星感和扩张)。结果:奥替溴铵组在2-4个月内的治疗反应率(主要疗效指标)显着高于安慰剂组(22.5%; P = 0.007)。在治疗的每个月中,溴化乙锭组的月反应率均高于安慰剂组(P <0.05)。与安慰剂相比,用奥替尼溴铵治疗的组每月和每周对单一终点的总反应(疼痛和不适的强度和频率,腹泻或便秘的严重程度,腹泻或便秘的严重程度和粪便的粘稠度)高得多。治疗组,差异从10%到20%。肠道习惯终点的亚组分析表明,腹泻患者还有其他好处。结论:目前对先前发表的一项研究进行的重新评估证实,溴化乙锭在治疗肠易激综合症方面比安慰剂更有效,在缓解疼痛和不适方面非常有效。

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