首页> 外文期刊>Journal of gastroenterology and hepatology >Efficacy of dioctahedral smectite in treating patients of diarrhea-predominant irritable bowel syndrome.
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Efficacy of dioctahedral smectite in treating patients of diarrhea-predominant irritable bowel syndrome.

机译:八面体蒙脱石治疗腹泻型肠易激综合征的疗效。

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Background and Aim: Dioctahedral smectite (DS) is natural adsorbent clay useful in treating acute diarrhea. The aim of this study was to determine DS efficacy on patients with diarrhea-predominant irritable bowel syndrome (D-IBS in a phase III-, 8-week-randomized, double-blind, placebo-controlled trial. Methods: The 104 patients who met the D-IBS Rome II criteria were randomized to receive either DS (n = 52) or placebo (n = 52) treatment for 8 weeks (three sachets daily). The primary efficacy endpoint was the changes of the visual analog scale (VAS) score of IBS overall disorder and pain/discomfort-related symptoms after treatment on days 28 and 56, respectively. Other outcome measures included improvement of bowel movement disorders. The therapeutic global response was assessed by the patients and investigators at each visit, as was drug safety. Results: Both treatments diminished overall disorder at each visit (P < 0.01), with respect to primary efficacy. This effect was further observed in DS-treated patients on day 56 (P = 0.0167). Placebo had no effect on the VAS score of pain/discomfort at any visit, whereas DS improved this score on days 28 and 56, respectively (P < 0.05). DS and placebo similarly diminished bowel disorders at each visit; however, only DS improved abdominal bloating (P < 0.01). The global therapeutic responses evaluated by the patients and investigators were similarly distributed. The study drug was well tolerated during the 8-week period. Conclusion: DS seems acceptable to treat D-IBS patients, particularly for pain-related symptoms.
机译:背景与目的:八面体蒙脱石(DS)是一种天然吸附性粘土,可用于治疗急性腹泻。这项研究的目的是确定在腹泻型肠易激综合征(D-IBS,III期,8周随机,双盲,安慰剂对照试验的患者)中的DS疗效。方法:104名患者符合D-IBS罗马II标准的患者随机接受DS(n = 52)或安慰剂(n = 52)治疗8周(每天3袋),主要疗效终点是视觉模拟量表(VAS)的变化)分别在第28天和第56天接受治疗的IBS总体障碍和与疼痛/不适相关的症状评分,其他结局指标包括肠蠕动障碍的改善,患者和研究者在每次就诊时评估了整体治疗反应,结果:两种治疗均降低了初次疗效(P <0.01),每次就诊的总体病症均得到缓解;在第56天,接受DS治疗的患者进一步观察到了这种效果(P = 0.0167)。疼痛/不适的VAS评分每次就诊时t,而DS分别在第28天和第56天改善了该评分(P <0.05)。 DS和安慰剂在每次访视时都可减少肠病。但是,只有DS改善了腹胀(P <0.01)。由患者和研究者评估的总体治疗反应也相似地分布。研究药物在8周内耐受良好。结论:DS似乎可以接受D-IBS患者的治疗,尤其是对于疼痛相关症状。

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