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Faecal microbiota transplantation in ulcerative colitis

Faecal Microbiota Transplantation in Ulcerative Colitis: an Interventional randomised single blind phase II trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN58082603
Enrollment
30
Registered
2015-07-24
Start date
2015-09-30
Completion date
Unknown
Last updated
2019-05-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ulcerative colitis Digestive System Ulcerative colitis

Interventions

Faecal microbiota transplant (FMT) will be administered by retention enema to patients either once only (group 1) or on five consecutive days (group 2). A third group with active disease will act as c

Sponsors

Abertawe Bro Morgannwg University LHB (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Newly diagnosed histologically confirmed ulcerative colitis with inflammation limited to the rectum or rectosigmoid (within 40cm of anal verge as measured by flexible sigmoidoscope) 2. Age 18 years and above 3. Able to give full informed written consent 4. Willing to return for sequential FMT dosing and endoscopic assessment 5. Not in receipt of standard medical treatment for colitis such as steroids or 5-ASA ie treatment naive

Exclusion criteria

Exclusion criteria: 1. Patients without a definitive diagnosis of UC (for example diagnosis of Crohn’s disease or infectious colitis) 2. Have colitis extending beyond 40cm from the anal verge 3. Have severe acute colitis (defined as greater than 6 bloodstained stools per 24 hrs with one of the following: pulse rate >90/ temperature >37.8’C/ haemoglobin 30) 5. Abdominal tenderness on examination 6. Already commenced standard medical therapy for UC 7. Contraindication to oral bowel preparation 8. Allergy to study antibiotics 9. Age less than 18 10. Patient is within a vunerable group 11. Are pregnant 12. Are immuno-suppressed e.g. transplant patient 13. Known communicable disease;,at least 2 weeks full recovery from infectious disease e.g. chickenpox 14. Systemic autoimmunity, or atopic diseases 15. Previous prosthetic implant (for example metallic heart valve, joint replacement, ventriculoperitoneal shunt, cardiac stent) 16. Chronic pain syndromes (for example: fibromyalgia, chronic fatigue) 17. Neurologic, neuro-developmental or neurodegenerative disorders 18. Depression (requiring therapy) 19. Obesity (BMI>35) 20. Malignancy 21. Use of antibiotics for any indication within the past 3 months 22. Foreign travel to areas of enteric disease prevalence within 3 months 23. High risk sexual behaviour (examples: sexual contact with anyone with HIV/HTLV/AIDS or hepatitis B/C carrier, men who have sex with men (MSM)) 24. Known exposure to HIV or hepatitis B/C 25. Current/previous use of injected drugs or intranasal cocaine 26. Tattooing, piercing, cosmetic botulinum toxin (Botox) or permanent makeup within 120 days (in line with Welsh Blood Transfusion guidelines) 27. Recent transfusion, transplant or skin graft 28. Risk factors for variant Creutzfeldt-Jakob disease e.g. blood transfusion or transplant after 1st January 1980

Design outcomes

Primary

MeasureTime frame
1. Remission of UC (mucosal healing) at 12 weeks as assessed by sigmoidoscopy, and patients response. Will also be measured utilising the Mayo scoring system for assessment of ulcerative colitis activity at 12 weeks, with remission defined as a Mayo score = 2 with an endoscopic Mayo score of 0. 2. Successful engraftment of donor faecal microbiota at 12 weeks as analysed by 16S sequencing

Secondary

MeasureTime frame
1. Rate of recruitment of patients 2. Disease specific severity scoring after treatment 3. Histological grading of colitis severity after treatment 4. Mucosal immunological response to treatment 5. Rate of development of adverse effects of FMT

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 23, 2026