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用溴化西托溴铵对肠易激综合征进行长期治疗:一项双盲安慰剂对照临床试验。

Longterm treatment of irritable bowel syndrome with cimetropium bromide: a double blind placebo controlled clinical trial.

作者信息

Dobrilla G, Imbimbo B P, Piazzi L, Bensi G

机构信息

Gastroenterology Division, General Regional Hospital, Bolzano, Italy.

出版信息

Gut. 1990 Mar;31(3):355-8. doi: 10.1136/gut.31.3.355.

Abstract

The aim of this study was to evaluate the efficacy of cimetropium bromide, a new antimuscarinic compound, in relieving symptoms of patients with irritable bowel syndrome over a three month period. Seventy consecutive outpatients were given cimetropium (50 mg tid) or placebo according to a double blind, randomised, parallel groups design. Symptoms were evaluated initially and at monthly intervals up to the end of the study period. One patient receiving placebo withdrew because of treatment failure. Pain score decreased by 40, 66, 85% in the cimetropium group, at the end of the first, second and third months respectively, compared with 26, 32 and 52% reductions among controls (p = 0.0005). At the end of treatment there was a 86% reduction in the number of abdominal pain episodes per day in the cimetropium group compared with 50% in the placebo group (p = 0.001). Constipation and diarrhoea scores decreased by 59 and 49% in the cimetropium treated patients, compared with 37 and 39% in controls, the differences between being not significant. At the end of the study 89% of the patients treated with cimetropium considered themselves as globally improved as opposed to 69% in the placebo group (p = 0.039). The corresponding 95% confidence intervals for the differences between the proportion of improved patients in the two groups were from 11% to 29%. Six patients taking cimetropium complained of slight dry mouth. The results of this study showed that cimetropium bromide is effective in relieving pain in patients with irritable bowel syndrome.

摘要

本研究旨在评估新型抗毒蕈碱化合物西托溴铵在三个月期间缓解肠易激综合征患者症状的疗效。按照双盲、随机、平行组设计,连续70名门诊患者被给予西托溴铵(50毫克,每日三次)或安慰剂。在研究期开始时及之后每月对症状进行评估。一名接受安慰剂治疗的患者因治疗失败退出。西托溴铵组在第一个月、第二个月和第三个月末疼痛评分分别下降了40%、66%和85%,而对照组分别下降了26%、32%和52%(p = 0.0005)。治疗结束时,西托溴铵组每日腹痛发作次数减少了86%,而安慰剂组减少了50%(p = 0.001)。西托溴铵治疗的患者便秘和腹泻评分分别下降了59%和49%,而对照组分别下降了37%和39%,两者差异不显著。研究结束时,89%接受西托溴铵治疗的患者认为自身整体状况改善,而安慰剂组为69%(p = 0.039)。两组改善患者比例差异的相应95%置信区间为11%至29%。六名服用西托溴铵的患者抱怨有轻微口干。本研究结果表明,西托溴铵对缓解肠易激综合征患者的疼痛有效。

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