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临床试验/NCT02154867
NCT02154867已完成2 期

Recalibrating Intestinal Microflora in IBS by Fecal Transplantation

University Hospital of North Norway2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2014年12月1日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
90
试验地点
2
主要终点
Change in subjective symptom score

研究概览

简要总结

Fecal Microbial Transplantation in Treatment of Irritable Bowel Syndrome; a Double Blinded Placebo Controlled Trial - the REFIT project

Irritable bowel syndrome (IBS) is a condition characterized by variable complaints like diarrhoea, bloating and abdominal pain, and may result in considerably reduced quality of life and increased sickness absence. The prevalence of IBS in the general population may be as high as 15 per cent depending on the diagnostic criteria used. The pathophysiology of IBS is poorly understood and theories of visceral hypersensitivity, micro-inflammation and other less well founded theories have been stated. So far, no measurement or test can affirm diagnosis, but exclusion of organic diseases in combination with a typical symptom pattern according to the Rome classification can set the diagnosis.

Earlier non-controlled case reports have shown a convincing effect of fecal microbial transplantation (FMT) in IBS patients. However, no placebo controlled trial has been performed in this condition. Changes in the gut microbiome may be an important factor in IBS pathogenesis. Microbiome analysis has revealed changes in microbiome composition that may trigger changes in visceral sensibility and pain perception.

The fecal microbial transplantation (FMT) procedure has been used primarily to treat clostridium difficile infections. Few minor side effects have been reported.

Hypothesis: IBS is caused by an imbalance of the gut microbiome that may be reset by transplanting a microbiome sample from a healthy donor.

Aim of study:

  • To test the clinical effect of FMT in patients with IBS
  • To describe the fecal microbiome in IBS patients
  • To describe changes in the fecal microbiome of IBS patients following FMT

The REFIT study will perform a randomized placebo-controlled double blinded trial of FMT on IBS according to the Rome 3 criteria. A study group of 60 IBS (diarrhoea variant) patients will recruited from general practice and allocated to active (30) or placebo (30) by block randomization. Donors will be 15 healthy volunteers with no risk behaviour and a pre-screening for communicable diseases will be performed.

Outcome measures will be clinical assessment by IBS-severity scoring system (IBS-SSS) at 0, 1, 3, 6, and 12 months. Microbiome analysis will be performed by metagenomic sequencing (University of Tromsø) at 0, 3, and 12 months for patients, and at inclusion for donors.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • for patients:
  • Patients with IBS-D according to Roma 3 criteria

排除标准

  • for patients:
  • Immunomodulating medication
  • Nocturnal abdominal pain
  • Constant abdominal pain
  • Alarm symptoms like rectal bleeding, weight loss, nightsweats
  • Symptomatic heart/vascular/lung disease
  • Renal failure
  • Known food allergy
  • Microscopic/collagenous colitis
  • non-compliant
  • Inclusion criteria for donors:
  • healthy volunteers
  • Exclusion criteria for donors
  • Tattoos, imprisoning or piercing last 3 months
  • Any history of chronic diarrhoea, constipation, inflammatory bowel disease, irritable bowel disease, colorectal polyps or cancer, immunosuppression, morbid obesity, metabolic syndrome, atopica, or fatigue
  • positive test for hepatitis B, C, HIV, treponema pallidum
  • sexual high risk habits
  • antibiotic treatment in the past 3 months

结局指标

主要结局

Change in subjective symptom score

时间窗: at 0 and 3 months

Comparison of Irritable bowel syndrome severity scoring system (IBS-SSS) grade assessment before and after fecal transplantation

次要结局

  • Microbiome profile change(at 0, 3 and 12 months)
  • Long term effects of fecal transplantation(at 12 months)
  • Safety of fecal transplantation in IBS(during study period (0-12 months))

研究者

发起方
University Hospital of North Norway
申办方类型
Other
责任方
Sponsor

研究点 (2)

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