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一项评估粪菌移植在儿童溃疡性结肠炎人群中的可行性和疗效的随机、安慰剂对照的初步研究方案:PediFETCh 试验。

Protocol for a randomised, placebo-controlled pilot study for assessing feasibility and efficacy of faecal microbiota transplantation in a paediatric ulcerative colitis population: PediFETCh trial.

机构信息

Division of Pediatric Gastroenterology & Nutrition, Department of Pediatrics, McMaster University, Hamilton, Canada.

McMaster Integrative Neuroscience Discovery and Study Graduate Program, McMaster University, Hamilton, Canada.

出版信息

BMJ Open. 2017 Aug 21;7(8):e016698. doi: 10.1136/bmjopen-2017-016698.

Abstract

INTRODUCTION

Ulcerative colitis (UC) is a chronic, relapsing condition characterised by colonic inflammation. Increasing prevalence in early-age diagnosis provides opportunities for additional complications in later life as a result of prolonged exposure to inflammatory and therapeutic insults, necessitating novel avenues for therapeutics which may result in fewer side effects. Faecal microbiota transplantation (FMT) has previously demonstrated potential therapeutic benefit in an adult randomised-controlled trial and several recurrent infection studies. This phase Ib pilot will be the first randomised, single-blinded, placebo-controlled trial to assess feasibility and patient outcomes in a paediatric inflammatory bowel disease (IBD) population.

METHODS AND ANALYSIS

Fifty patients will be randomised 1:1 to receive normal saline control or active sample. Enema administrations will be performed two times per week for 6 weeks, followed at a 6-month follow-up period. Feasibility outcomes will include measures of patient eligibility, recruitment, willingness to participate, samples collections, hospitalizations and drop-out rate. Improvements in disease symptoms will determine the efficacy of treatment. Clinical disease scores will be taken throughout the study period using the Paediatric Ulcerative Colitis Activity Index (PUCAI). Monitoring of inflammatory markers in blood and stool will be performed at regular intervals. Microbiome analysis will be conducted on stool samples collected throughout the trials period. Imaging and endoscopic surveillance will be conducted if clinically necessary.

ETHICS AND DISSEMINATION

Ethics was obtained from local hospital research ethics boards across all three sites. Health Canada and FDA approval was obtained for the use of an Investigatory New Drug product. Results from this trial will be presented in international conferences and published in peer-review journals.

TRIAL REGISTRATION NUMBER

Trial registration number: NCT02487238; preresults.

摘要

简介

溃疡性结肠炎(UC)是一种慢性、复发性疾病,其特征为结肠炎症。早期诊断的发病率不断增加,这使得患者在以后的生活中由于长期暴露于炎症和治疗性刺激,可能会出现更多的并发症,这就需要新的治疗方法,以减少副作用。粪便微生物群移植(FMT)在一项成人随机对照试验和几项复发性感染研究中已显示出潜在的治疗益处。这项 Ib 期试验将是第一项在儿童炎症性肠病(IBD)人群中评估可行性和患者结局的随机、单盲、安慰剂对照试验。

方法和分析

将 50 名患者随机分为 1:1 组,分别接受生理盐水对照或活性样本治疗。灌肠治疗将每周进行两次,持续 6 周,然后在 6 个月的随访期进行。可行性结果将包括患者合格性、招募、参与意愿、样本采集、住院和脱落率的测量。疾病症状的改善将决定治疗的疗效。整个研究期间将使用小儿溃疡性结肠炎活动指数(PUCAI)评估临床疾病评分。将定期监测血液和粪便中的炎症标志物。将对整个试验期间收集的粪便样本进行微生物组分析。如果临床需要,将进行影像学和内镜监测。

伦理和传播

所有三个地点的当地医院研究伦理委员会都获得了伦理批准。加拿大卫生部和 FDA 批准了一种新药产品的使用。该试验的结果将在国际会议上公布,并发表在同行评议期刊上。

试验注册号

试验注册号:NCT02487238;preresults。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ca6/5629651/be69bbf213cf/bmjopen-2017-016698f01.jpg

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