Fecal Microbial Transplantation in Treatment of Irritable Bowel Syndrome; a Double Blinded Placebo Controlled Trial. (REFIT)
Primary Purpose
Irritable Bowel Syndrome
Status
Completed
Phase
Phase 2
Locations
Norway
Study Type
Interventional
Intervention
Fecal transplantation
Placebo fecal transplant
Sponsored by
About this trial
This is an interventional treatment trial for Irritable Bowel Syndrome focused on measuring IBS-D, FMT, metagenomics, gut microbiome
Eligibility Criteria
Inclusion Criteria for patients:
- Patients with IBS-D according to Roma 3 criteria
Exclusion Criteria 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
- BMI <18
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
Sites / Locations
- University Hospital of North Norway
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Fecal transplantation
Placebo fecal transplantation
Arm Description
Fecal transplantation of freshly prepared feces from healthy donor. Application by colonoscope in proximal half of colon.
Sham transplant subject's own feces. Application by colonoscope in proximal part of colon.
Outcomes
Primary Outcome Measures
Change in subjective symptom score
Comparison of Irritable bowel syndrome severity scoring system (IBS-SSS) grade assessment before and after fecal transplantation
Secondary Outcome Measures
Microbiome profile change
Characterization of fecal microbiome by metagenomic analysis before and after intervention
Long term effects of fecal transplantation
Assessment of symptom burden by IBS-SSS
Safety of fecal transplantation in IBS
Registration of any adverse events. If any serious adverse events are encountered, the study group and local ethics committee will evaluate if study should be terminated.
Full Information
NCT ID
NCT02154867
First Posted
April 10, 2014
Last Updated
January 12, 2017
Sponsor
University Hospital of North Norway
1. Study Identification
Unique Protocol Identification Number
NCT02154867
Brief Title
Fecal Microbial Transplantation in Treatment of Irritable Bowel Syndrome; a Double Blinded Placebo Controlled Trial.
Acronym
REFIT
Official Title
Recalibrating Intestinal Microflora in IBS by Fecal Transplantation
Study Type
Interventional
2. Study Status
Record Verification Date
January 2015
Overall Recruitment Status
Completed
Study Start Date
December 2014 (undefined)
Primary Completion Date
October 2016 (Actual)
Study Completion Date
December 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital of North Norway
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome
Keywords
IBS-D, FMT, metagenomics, gut microbiome
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
90 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Fecal transplantation
Arm Type
Experimental
Arm Description
Fecal transplantation of freshly prepared feces from healthy donor. Application by colonoscope in proximal half of colon.
Arm Title
Placebo fecal transplantation
Arm Type
Placebo Comparator
Arm Description
Sham transplant subject's own feces. Application by colonoscope in proximal part of colon.
Intervention Type
Biological
Intervention Name(s)
Fecal transplantation
Other Intervention Name(s)
Fecal microbial transplantation
Intervention Description
Preparation of flesh feces by blending in 0.9 % saline and crude filtering. The solution is applied in proximal colon of IBS patient by colonoscopy after standard bowel preparation.
Intervention Type
Other
Intervention Name(s)
Placebo fecal transplant
Intervention Description
Fecal transplantation with own feces
Primary Outcome Measure Information:
Title
Change in subjective symptom score
Description
Comparison of Irritable bowel syndrome severity scoring system (IBS-SSS) grade assessment before and after fecal transplantation
Time Frame
at 0 and 3 months
Secondary Outcome Measure Information:
Title
Microbiome profile change
Description
Characterization of fecal microbiome by metagenomic analysis before and after intervention
Time Frame
at 0, 3 and 12 months
Title
Long term effects of fecal transplantation
Description
Assessment of symptom burden by IBS-SSS
Time Frame
at 12 months
Title
Safety of fecal transplantation in IBS
Description
Registration of any adverse events. If any serious adverse events are encountered, the study group and local ethics committee will evaluate if study should be terminated.
Time Frame
during study period (0-12 months)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria for patients:
Patients with IBS-D according to Roma 3 criteria
Exclusion Criteria 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
BMI <18
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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rasmus Goll, PhD
Organizational Affiliation
University Hospital of North Norway
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Per C Valle, PhD
Organizational Affiliation
University Hospital of North Norway
Official's Role
Study Director
Facility Information:
Facility Name
University Hospital of North Norway
City
Harstad
ZIP/Postal Code
9406
Country
Norway
12. IPD Sharing Statement
Citations:
PubMed Identifier
32991818
Citation
Goll R, Johnsen PH, Hjerde E, Diab J, Valle PC, Hilpusch F, Cavanagh JP. Effects of fecal microbiota transplantation in subjects with irritable bowel syndrome are mirrored by changes in gut microbiome. Gut Microbes. 2020 Nov 9;12(1):1794263. doi: 10.1080/19490976.2020.1794263.
Results Reference
derived
PubMed Identifier
29100842
Citation
Johnsen PH, Hilpusch F, Cavanagh JP, Leikanger IS, Kolstad C, Valle PC, Goll R. Faecal microbiota transplantation versus placebo for moderate-to-severe irritable bowel syndrome: a double-blind, randomised, placebo-controlled, parallel-group, single-centre trial. Lancet Gastroenterol Hepatol. 2018 Jan;3(1):17-24. doi: 10.1016/S2468-1253(17)30338-2. Epub 2017 Nov 1.
Results Reference
derived
Learn more about this trial
Fecal Microbial Transplantation in Treatment of Irritable Bowel Syndrome; a Double Blinded Placebo Controlled Trial.
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