Irritable Bowel SyndromeNCT06171126
Donor Selection for Faecal Microbiota Transplantation in Irritable Bowel Syndrome
A study testing Faeces from donor A, Faeces from donor B and Faeces from donor C in people with Irritable Bowel Syndrome, run by Haukeland University Hospital at 3 sites in Norway.
Trial summary
Five hundred patients are randomized 1:1:1:1 into placebo (own feces), or receiving 90 g fecal transplant from donor A, donor B or donor C. The fecal transplant is administered to the distal duodenum via the working channel of a gastroscope. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Irritable Bowel Syndrome
- What is being tested?
- Faeces from donor A, Faeces from donor B and Faeces from donor C
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 500 participants
- Where
- 3 sitesNorway
- Study dates
- 15 Feb 2024to 31 Aug 2028
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 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-SSS questionnaire
Who cannot join
- Pregnant, women planning pregnancy or lactating women.
- The use of antibiotics or probiotics within 1
- month prior to FMT.
- Having undergone any abdominal surgery, with
- the exception of appendectomy, cholecystectomy,
- caesarean section and hysterectomy.
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- Previous treatment with FMT.
- Immunocompromised patients including those being
- treated by immunosuppressive medications.
- Patients with co-morbidity such as kidney failure,
- diabetes or chronic heart disease.
- Patients with serious psychiatric disorders
- or alcohol or drug abuse.
Trial locations and contacts
3 sites in 1 country.
Norway3 sites
Helse Møre og Romsdal HF
Ålesund
Haukeland University Hospital
Bergen, Vestland, 5021
Diakonhjemmet
Oslo
About this study
Official title: The Role of Donor Selection on the Outcome of Faecal Microbiota Transplantation (FMT) in Patients With Irritable Bowel Syndrome: a Multi-center Randomised, Double-blinded Placebo-controlled Study
Five hundred patients are randomized 1:1:1:1 into placebo (own feces), or receiving 90 g fecal transplant from donor A, donor B or donor C. The fecal transplant is administered to the distal duodenum via the working channel of a gastroscope. The patients shall complete 6 questionnaires measuring symptoms, fatigue, quality of life, stool form and diet intake at the baseline and at the end point of the trial and provide a feces sample at the baseline, and at 3, 6 and 12 months after FMT. Dysbiosis and fecal bacterial profile are determined by using 16S rRNA gene PCR DNA amplification/probe hybridization covering regions V3-V9.
Read the detailed description
Study Description Brief Summary: Five hundred patients are randomized1:1:1:1 into placebo (own feces), receiving 90 g fecal transplant from donor A, donor B or donor C. The fecal transplant is administered to distal duodenum via working channel of a gastroscope. The patients shall complete 5 questionnaires measuring symptoms, fatigue, quality of life and diet intake at the baseline and at the end point of the trial and provide 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 PCR DNA amplification/probe hybridization covering regions V3-V9.
Detailed Description: Patients: Five hundred patients who fulfil Rome IV criteria for irritable bowel syndrome (IBS) shall be included in the study. All IBS subtypes shall be included with the exception of IBS-U. Donors: The investigators have selected 3 donors (A, B and C) according to the criteria used in their previous randomised double-blind, placebo-controlled study. These criteria included: being a healthy man or woman with no history of disease and no use of medications, aged 20-50 years, being a non-smoker, and exercising regularly. They were borne by vaginal delivery and breastfed. They were treated only a few times with antibiotics during their life. They are screened according to the European guidelines for donors for FMT. Before they are accepted as donors, the bacterial profile and dysbiosis were analysed in a faecal sample using the GA-map dysbiosis test, with a dysbiosis index (DI)= 1, indicating normobiosis. Their feces shall be tested every third month during the trial to exclude communicable disease. Donor A is a male aged 41 years, donor B is a female aged 31 and donor C is a male aged 35.
Protocol: The patients are randomized 1:1:1:1 into placebo (to receive their own feces), to receive 90 g fecal transplant from donor A, from donor B or donor C. Fecal transplant is administered to the distal duodenum via the working channel of a gastroscope. The patients shall complete 5 questionnaires and deliver fecal samples at the baseline, and at 3 , 6 , and 12 months after FMT. Feces collection, preparation and administration: Faeces from both the donors and patients shall be collected and stored at - 80ºC. Frozen donor faeces shall be thawed in the refrigerator at 4ºC, and dissolved in 200 mL of 4ºC cold 0.9% sterile saline. The dissolved stool is administrated to the patients, after an overnight fast, through the working channel of a gastroduodenoscope in the pars descendens of the duodenum always distal to the papilla of Vater. Questionnaires
- IBS Symptom Severity Scale (IBS-SSS).
- Birmingham Symptom Scale.
- Fatigue Assessment Scale (FAS).
- IBS-quality of life (IBSQoL) Questionnaire.
- A 5-points subjective global assessment scale
- Bristol Stool Form Scale
Bacterial analysis: Fecal bacterial analysis is performed using a 16S rRNA gene PCR DNA amplification/probe hybridization technique covering regions V3-V9. DNA extraction is done by using magnetic beads. DI is based on 174 DNA probes targeting more than 300 bacterial strains based on their 16S rRNA sequence in seven variable regions (V3-V9). 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).
- Conditions
- Irritable Bowel Syndrome
- Being tested
- Placebo, Faeces from donor A, Faeces from donor B, Faeces from donor C
- Keywords
- Fecal microbiota transplantation, Intestinal microbiota, Donor, Dysbiosis, Abdominal symptom, Fatigue, Quality of life
- Medical subject headings
- Irritable Bowel Syndrome, Dysbiosis, Fatigue
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PlaceboDietary supplement
By gastroscopy
Faeces from donor ADietary supplement
By gastroscopy
Faeces from donor BDietary supplement
By gastroscopy
Faeces from donor CDietary supplement
By gastroscopy
| Study group | Role | What they receive |
|---|---|---|
| Placebo | Placebo comparator | Own faeces instilled to the small intestine during gastroscopy Receives: Dietary Supplement: Placebo |
| Arm A | Experimental | 90g of faeces from Donor A is instilled to the small intestine during gastroscopy Receives: Dietary Supplement: Faeces from donor A |
| Arm B | Experimental | 90g of faeces from Donor B is instilled to the small intestine during gastroscopy Receives: Dietary Supplement: Faeces from donor B |
| Arm C | Experimental | 90g of faeces from Donor C is instilled to the small intestine during gastroscopy Receives: Dietary Supplement: Faeces from donor C |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in IBS-Severity Scoring System total score
Irritable Bowel Syndrome-Severity Scoring System (IBS-SSS) is a visual analogue scale questionnaire with a total score between 0 and 500 points, with "0" meaning no symptom and higher scores meaning increasing severity. A decrease in total score by ≥50 points is considered as a meaningful response.
Measured: 12 months after FMT
Secondary outcomes (1)
Change in 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
Measured: 12 months after FMT
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted14 Dec 2023
- Study start15 Feb 2024
- Primary completion31 Dec 2027 (estimated)
- Study completion31 Aug 2028 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Irritable Bowel SyndromeStudies of the same condition, open and under way.
- More trials run by Haukeland University HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 500 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Haukeland University Hospital
- Sponsor type
- University, hospital or other
- Collaborators
- University of Bergen
- Responsible party
- Sponsor
- Investigators
- Jan G Hatlebakk, PhD, Study chair, Haukeland University Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06171126
- Sponsor's protocol ID
- 630339
- Status last verified
- Sep 2025
- First submitted
- 6 Dec 2023
- Last updated
- 22 Sep 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes: After the completion of the study, study data may be made available to other researchers after contacting the primary investigator
Study at a glance
From the registry record, last updated by the sponsor on 22 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Role of Donor Selection on the Outcome of Faecal Microbiota Transplantation (FMT) in Patients With Irritable Bowel Syndrome: a Multi-center Randomised, Double-blinded Placebo-controlled Study
- ClinicalTrials.gov ID
- NCT06171126
- Acronym / sponsor ID
- 630339
- Conditions
- Irritable Bowel Syndrome
- Keywords
- Fecal microbiota transplantation, Intestinal microbiota, Donor, Dysbiosis, Abdominal symptom, Fatigue, Quality of life
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 500 participants (estimated)
- Lead sponsor
- Haukeland University HospitalUniversity, hospital or other
- Collaborators
- University of Bergen
- Study start
- 15 Feb 2024 (actual)
- Primary completion
- 31 Dec 2027 (estimated)
- Study completion
- 31 Aug 2028 (estimated)
- First posted
- 14 Dec 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Five hundred patients are randomized 1:1:1:1 into placebo (own feces), or receiving 90 g fecal transplant from donor A, donor B or donor C. The fecal transplant is administered to the distal duodenum via the working channel of a gastroscope. The patients shall complete 6 questionnaires measuring symptoms, fatigue, quality of life, stool form and diet intake at the baseline and at the end point of the trial and provide a feces sample at the baseline, and at 3, 6 and 12 months after FMT. Dysbiosis and fecal bacterial profile are determined by using 16S rRNA gene PCR DNA amplification/probe hybridization covering regions V3-V9.
Detailed description
Study Description Brief Summary: Five hundred patients are randomized1:1:1:1 into placebo (own feces), receiving 90 g fecal transplant from donor A, donor B or donor C. The fecal transplant is administered to distal duodenum via working channel of a gastroscope. The patients shall complete 5 questionnaires measuring symptoms, fatigue, quality of life and diet intake at the baseline and at the end point of the trial and provide 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 PCR DNA amplification/probe hybridization covering regions V3-V9.
Detailed Description: Patients: Five hundred patients who fulfil Rome IV criteria for irritable bowel syndrome (IBS) shall be included in the study. All IBS subtypes shall be included with the exception of IBS-U. Donors: The investigators have selected 3 donors (A, B and C) according to the criteria used in their previous randomised double-blind, placebo-controlled study. These criteria included: being a healthy man or woman with no history of disease and no use of medications, aged 20-50 years, being a non-smoker, and exercising regularly. They were borne by vaginal delivery and breastfed. They were treated only a few times with antibiotics during their life. They are screened according to the European guidelines for donors for FMT. Before they are accepted as donors, the bacterial profile and dysbiosis were analysed in a faecal sample using the GA-map dysbiosis test, with a dysbiosis index (DI)= 1, indicating normobiosis. Their feces shall be tested every third month during the trial to exclude communicable disease. Donor A is a male aged 41 years, donor B is a female aged 31 and donor C is a male aged 35.
Protocol: The patients are randomized 1:1:1:1 into placebo (to receive their own feces), to receive 90 g fecal transplant from donor A, from donor B or donor C. Fecal transplant is administered to the distal duodenum via the working channel of a gastroscope. The patients shall complete 5 questionnaires and deliver fecal samples at the baseline, and at 3 , 6 , and 12 months after FMT. Feces collection, preparation and administration: Faeces from both the donors and patients shall be collected and stored at - 80ºC. Frozen donor faeces shall be thawed in the refrigerator at 4ºC, and dissolved in 200 mL of 4ºC cold 0.9% sterile saline. The dissolved stool is administrated to the patients, after an overnight fast, through the working channel of a gastroduodenoscope in the pars descendens of the duodenum always distal to the papilla of Vater. Questionnaires
- IBS Symptom Severity Scale (IBS-SSS).
- Birmingham Symptom Scale.
- Fatigue Assessment Scale (FAS).
- IBS-quality of life (IBSQoL) Questionnaire.
- A 5-points subjective global assessment scale
- Bristol Stool Form Scale
Bacterial analysis: Fecal bacterial analysis is performed using a 16S rRNA gene PCR DNA amplification/probe hybridization technique covering regions V3-V9. DNA extraction is done by using magnetic beads. DI is based on 174 DNA probes targeting more than 300 bacterial strains based on their 16S rRNA sequence in seven variable regions (V3-V9). 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).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| Placebo | Placebo comparator | Dietary Supplement: PlaceboOwn faeces instilled to the small intestine during gastroscopy |
| Arm A | Experimental | Dietary Supplement: Faeces from donor A90g of faeces from Donor A is instilled to the small intestine during gastroscopy |
| Arm B | Experimental | Dietary Supplement: Faeces from donor B90g of faeces from Donor B is instilled to the small intestine during gastroscopy |
| Arm C | Experimental | Dietary Supplement: Faeces from donor C90g of faeces from Donor C is instilled to the small intestine during gastroscopy |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- 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
Key exclusion criteria (13 listed)
- Pregnant, women planning pregnancy or lactating women.
- The use of antibiotics or probiotics within 1
- month prior to FMT.
- Having undergone any abdominal surgery, with
- the exception of appendectomy, cholecystectomy,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| PlaceboBy gastroscopy | Dietary supplement | Placebo |
| Faeces from donor ABy gastroscopy | Dietary supplement | Arm A |
| Faeces from donor BBy gastroscopy | Dietary supplement | Arm B |
| Faeces from donor CBy gastroscopy | Dietary supplement | Arm C |
Primary outcome
Change in IBS-Severity Scoring System total score
Time frame: 12 months after FMT
Irritable Bowel Syndrome-Severity Scoring System (IBS-SSS) is a visual analogue scale questionnaire with a total score between 0 and 500 points, with "0" meaning no symptom and higher scores meaning increasing severity. A decrease in total score by ≥50 points is considered as a meaningful response.
1 secondary outcome
Change in dysbiosis index
Time frame: 12 months after FMT
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 22 Sep 2025.
- Individual participant dataSharing planned: Yes. After the completion of the study, study data may be made available to other researchers after contacting the primary investigator
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Jan G Hatlebakk, PhD study chair
Haukeland University Hospital
3 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Faeces from donor A, Faeces from donor B and Faeces from donor C in people with Irritable Bowel Syndrome, run by Haukeland University Hospital at 3 sites in Norway.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 13 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: under way, not looking for participants, as of the sponsor's last update on 22 Sep 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 3 sites in Norway. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in IBS-Severity Scoring System total score (time frame: 12 months after FMT). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 22 Sep 2025.