Faecal Microbiota Transplantation (FMT) in Patients With IBSmechanism(s) of Action
Primary Purpose
Irritable Bowel Syndrome
Status
Completed
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
Feces
Sponsored by
About this trial
This is an interventional treatment trial for Irritable Bowel Syndrome focused on measuring Fecal microbiota transplantation, Intestinal microbiota, Donor, Dysbiosis, Abdominal symptom, Fatigue, Quality of life
Eligibility Criteria
Inclusion Criteria:
- Patients who fulfil Rome IV criteria for the diagnosis of IBS.
- Patients were investigated to exclude other gastrointestinal organic cause(s).
- Moderate-to-severe IBS symptoms, as indicated by a score of ≥175 on the IBS Severity Scoring System (IBS-SSS).
Exclusion Criteria:
- Pregnant or lactating women.
- The use of antibiotics or probiotics within 1 month prior to FMT.
- Immunocompromised patients defined as those treated by immune- suppressive medications.
- Patients with co-morbidity such as kidney failure or chronic heart disease.
- System disease such as diabetes.
- Patients with serious psychiatric disorders or drug abuse.
Sites / Locations
- Helse Fonna
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Smal intestine once
Small intestine twice
Large intestine once
Arm Description
90-g fecal transplant given into the small intestine once.
90-g fecal transplant given into the small intestine twice with 1 week interval.
90-g fecal transplant given into the large intestine once.
Outcomes
Primary Outcome Measures
Change in IBS-SSS total score
Irritable bowel syndrome-symptom severity score (IBS-SSS) is a visual analogue scale questionnaire with a maximum score of 500 points. A decrease in total score by ≥50 points is considered as a response.
Secondary Outcome Measures
Change in the Dysbiosis index
Dysbiosis index (DI) is a 5 -scale index. A DI above 2 shows a microbiota profile that differs from that of the normobiotic reference collection (DI 1-2: non-dysbiosis, DI 3: moderate, DI 4-5: severe dysbiosis)
Full Information
NCT ID
NCT04236843
First Posted
January 15, 2020
Last Updated
August 17, 2023
Sponsor
Helse Fonna
Collaborators
University of Bergen
1. Study Identification
Unique Protocol Identification Number
NCT04236843
Brief Title
Faecal Microbiota Transplantation (FMT) in Patients With IBSmechanism(s) of Action
Official Title
Faecal Microbiota Transplantation (FMT) in Patients With Irritable Bowel Syndrome (IBS): Optimizing the Treatment and Its Mechanism(s) of Action
Study Type
Interventional
2. Study Status
Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
February 3, 2020 (Actual)
Primary Completion Date
March 25, 2022 (Actual)
Study Completion Date
March 25, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Helse Fonna
Collaborators
University of Bergen
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Two hundrad patients are randomized to either 90 g transplant, 90 g transplant twice with 1week interval into the distal small intestine via working channel of a gastroscope, or to 90 g transplant into the coecum of the colon via working channel of a colonoscope. The patients shall complete 5 questionnaires measuring symptoms, fatigue and quality of life and collect a feces sample at the baseline, and at 3, 6 and 12 months after FMT. Dysbiosis and fecal bacterial are determined by using 16S rRNA gene.
Detailed Description
Patients Two hundrad patients who fulfil Rome IV criteria for irritable bowel syndrome (IBS) shall be included in the study. All the IBS subtypes shall be included.
Donor Investigators are going to use the same super-donor they used in their previous randomised double-blind, placebo-controlled study. The donor is athletic Caucasian man aging 36 years. He is non-smoker and is completely healthy without any medication and with a BMI of 23.5. He is not relative to any of the patients in the trial. He was borne by vaginal delivery and breastfeed. He was treated 3 times with antibiotics during his life. He trains 5 times weekly an hour each time. He took regularly dietary supplements rich in proteins, vitamins, fibres and minerals that made his diet richer than average in these substances. He was screened according to the guidelines for donors for FMT. Before he was accepted as a donor the microbiota was analysed in a faecal sample using GA-map Dysbiosis test. The analysis revealed a dysbiosis index (DI)= 1, indicating normobiosysis. In addition, he had excess of bacteria belonging to the Firmicutes. His faeces shall be tested every third moth during the trial.
Protocol
The patients are randomized to either 90 g transplant, 90 g transplant twice with 1week interval into the distal small intestine, or to 90 g transplant into the coecum of the colon. The patients shall complete 5 questionnaires and deliver fecal samples at the baseline, and at 3 , 6 , and 12 months after FMT.
Faeces collection, preparation and administration Faeces from both the donor and patients shall be collected and stored at - 80•. Frozen faeces shall be thawed and each 30 g is dissolved in 30 mL of 0.9% sterile saline. The dissolved stool administrated to the patients, after overnight fast, through working channel of gastroduodeno-scope in pars descendent duodenum distal to the papilla of Vater or to the coecum through working channel of a colonoscope.
Analysis Questionnaires
IBS symptom severity Scale (IBS-SSS).
Birmingham Symptom scale.
IBS-quality of life (IBSQo) Questionnaire.
Short form of Nepean Dyspepsia Index (SF-NDI).
Fatigue Assessment Scale (FAS).
Microbiome analysis Gut microbiota analysis is performed using the Genetic analysis-mapTM Dysbiosis test (Genetic Analysis AS, Oslo, Norway) by algorithmically assessing faecal bacterial abundance and profile (dysbiosis index, DI), and potential deviation in the microbiome from normobiosis. GA-map test is based on faecal homogenization, mechanical bacterial cell disruption and automated total bacterial genomic DNA extraction using magnetic beads. DI is based on 54 DNA probes targeting more than 300 bacterial strains based on their 16S rRNA sequence in seven variable regions (V3-V9). Twenty-six bacteria probes are species specific, 19 detect bacteria on genus level, and 9 probes detect bacteria at higher taxonomic levels. Probe labelling is by single nucleotide extension and hybridization to complementary probes coupled to magnetic beads, and signal detection by using BioCode 1000A 128-Plex Analyser (Applied BioCode, Santa Fe Springs, CA, USA). A DI above 2 shows a microbiota profile that differs from that of the normobiotic reference collection (DI 1-2: non-dysbiosis, DI: moderate, DI 4-5: severe dysbiosis).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Irritable Bowel Syndrome
Keywords
Fecal microbiota transplantation, Intestinal microbiota, Donor, Dysbiosis, Abdominal symptom, Fatigue, Quality of life
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
186 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Smal intestine once
Arm Type
Active Comparator
Arm Description
90-g fecal transplant given into the small intestine once.
Arm Title
Small intestine twice
Arm Type
Active Comparator
Arm Description
90-g fecal transplant given into the small intestine twice with 1 week interval.
Arm Title
Large intestine once
Arm Type
Active Comparator
Arm Description
90-g fecal transplant given into the large intestine once.
Intervention Type
Dietary Supplement
Intervention Name(s)
Feces
Intervention Description
Feces from healthy donor
Primary Outcome Measure Information:
Title
Change in IBS-SSS total score
Description
Irritable bowel syndrome-symptom severity score (IBS-SSS) is a visual analogue scale questionnaire with a maximum score of 500 points. A decrease in total score by ≥50 points is considered as a response.
Time Frame
12 months after FMT
Secondary Outcome Measure Information:
Title
Change in the Dysbiosis index
Description
Dysbiosis index (DI) is a 5 -scale index. A DI above 2 shows a microbiota profile that differs from that of the normobiotic reference collection (DI 1-2: non-dysbiosis, DI 3: moderate, DI 4-5: severe dysbiosis)
Time Frame
12 months after FMT
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients who fulfil Rome IV criteria for the diagnosis of IBS.
Patients were investigated to exclude other gastrointestinal organic cause(s).
Moderate-to-severe IBS symptoms, as indicated by a score of ≥175 on the IBS Severity Scoring System (IBS-SSS).
Exclusion Criteria:
Pregnant or lactating women.
The use of antibiotics or probiotics within 1 month prior to FMT.
Immunocompromised patients defined as those treated by immune- suppressive medications.
Patients with co-morbidity such as kidney failure or chronic heart disease.
System disease such as diabetes.
Patients with serious psychiatric disorders or drug abuse.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Magdy El-Salhy, MD,PhD
Organizational Affiliation
Helse Fonna
Official's Role
Study Chair
Facility Information:
Facility Name
Helse Fonna
City
Haugesund
ZIP/Postal Code
5504
Country
Norway
12. IPD Sharing Statement
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Faecal Microbiota Transplantation (FMT) in Patients With IBSmechanism(s) of Action
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