...
首页> 外文期刊>Trials >Treatment of irritable bowel syndrome with diarrhoea using titrated ondansetron (TRITON): study protocol for a randomised controlled trial
【24h】

Treatment of irritable bowel syndrome with diarrhoea using titrated ondansetron (TRITON): study protocol for a randomised controlled trial

机译:滴定的恩丹西酮(TRITON)治疗腹泻型肠易激综合症:一项随机对照试验的研究方案

获取原文
           

摘要

Irritable bowel syndrome with diarrhoea (IBS-D) affects up to 4% of the general population. Symptoms include frequent, loose, or watery stools with associated urgency, resulting in marked reduction of quality of life and loss of work productivity. Ondansetron, a 5HT3 receptor antagonist, has had an excellent safety record for over 20?years as an antiemetic, yet is not widely used in the treatment of IBS-D. It has, however, been shown to slow colonic transit and in a small randomised, placebo-controlled, cross-over pilot study, benefited patients with IBS-D. This trial is a phase III, parallel group, randomised, double-blind, multi-centre, placebo-controlled trial, with embedded mechanistic studies. Participants (n = 400) meeting Rome IV criteria for IBS-D will be recruited from outpatient and primary care clinics and by social media to receive either ondansetron (dose titrated up to 24?mg daily) or placebo for 12?weeks. Throughout the trial, participants will record their worst abdominal pain, worst urgency, stool frequency, and stool consistency on a daily basis. The primary endpoint is the proportion of “responders” in each group, using Food and Drug Administration (FDA) recommendations. Secondary endpoints include pain intensity, stool consistency, frequency, and urgency. Mood and quality of life will also be assessed. Mechanistic assessments will include whole gut transit, faecal tryptase and faecal bile acid concentrations at baseline and between weeks 8 and 11. A subgroup of participants will also undergo assessment of sensitivity (n?=?80) using the barostat, and/or high-resolution colonic manometry (n?=?40) to assess motor patterns in the left colon and the impact of ondansetron. The TRITON trial aims to assess the effect of ondansetron across multiple centres. By defining ondansetron’s mechanisms of action we hope to better identify patients with IBS-D who are likely to respond. ISRCTN, ISRCTN17508514 , Registered on 2 October 2017.
机译:腹泻型肠易激综合症(IBS-D)影响普通人群的4%。症状包括频繁,稀疏或水汪汪的大便以及相关的紧迫性,导致生活质量显着下降和工作效率下降。恩丹西酮是5HT3受体拮抗剂,作为止吐药已有20多年的优异安全记录,但尚未广泛用于IBS-D的治疗。然而,它已被证明可以减缓结肠运输,在一项小型的,随机,安慰剂对照,交叉试验研究中,IBS-D患者受益。该试验是一项III期,平行组,随机,双盲,多中心,安慰剂对照试验,并进行了嵌入式机理研究。符合IBS-D罗马IV标准的参与者(n = 400)将从门诊和初级保健诊所招募,并通过社交媒体招募接受恩丹西酮(每天滴定剂量至24 mg)或安慰剂,持续12周。在整个试验过程中,参与者将每天记录他们最严重的腹痛,最紧迫性,大便次数和大便稠度。主要终点是按照美国食品药品监督管理局(FDA)的建议,每组中“响应者”的比例。次要终点包括疼痛强度,大便稠度,频率和尿急。情绪和生活质量也将得到评估。机械评估包括基线时以及第8周和第11周之间的整个肠道运输,粪便类胰蛋白酶和粪便胆汁酸浓度。参加者的一个亚组也将使用恒压器和/或高剂量法进行敏感性评估(n?=?80)。分辨率结肠测压法(n≥40),以评估左结肠的运动模式和恩丹西酮的影响。 TRITON试验旨在评估恩丹西酮在多个中心的疗效。通过定义恩丹西酮的作用机制,我们希望能更好地识别出可能应答的IBS-D患者。 ISRCTN,ISRCTN17508514,于2017年10月2日注册。

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号