Actively Recruiting
Superdonor FMT in Patients With Ulcerative Colitis
Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2026-03-19
42
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In the last decades fecal microbiota transplantation (FMT) has been established as a highly effective option in the treatment of recurrent Clostridioides difficile infection (rCDI), with a success rate of nearly 90%. For this reason, it is recommended by international guidelines as a treatment option for this indication in clinical practice. Recently, a considerable body of evidences, suggest FMT as an effective and safe treatment in patients affected by Ulcerative Colitis (UC). In a recent meta-analysis of 324 subjects with UC, 30.4% of patients achieved both clinical and endoscopic remission after FMT compared to placebo (9.8%, P\<0.00001). However, among the various published trials there is a fair variability in terms of methods and results, which are not comparable to those obtained in the rCDI. Nowadays, one of the most critical factors involved in the effectiveness of FMT in UC patients, is the choice of the donor. In addition, several studies have shown that some donors are associated with a higher clinical response rate than others. This hypothesis has been demonstrated in patients affected by irritable bowel syndrome, in which the use of a super-donor (a healthy person who has the predictive clinical and lifestyle characteristics of a healthy microbiota, and with a microbial profile associated with favorable clinical conditions) resulted in significantly higher clinical efficacy rates than placebo, similar to those obtained in rCDI (89%). Currently, studies that explored the efficacy of the super-donor FMT in UC patients are not yet available. Aim of this study is to investigate the efficacy of super - donor FMT, compared with placebo FMT, in the treatment of UC. The investigators will randomize adult patients with a recent diagnosis of UC to FMT from super - donors or placebo, by colonoscopy (first infusion) and capsules administration. Then, patients will be followed up 2 months after FMT.
CONDITIONS
Official Title
Superdonor FMT in Patients With Ulcerative Colitis
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 75 years old
- Mild to moderate Ulcerative Colitis with total Mayo score 3-10 and endoscopic subscore 1
- Stable maintenance therapy for more than 4 weeks with Aminosalicylates or more than 6 weeks with immunosuppressants or biologics
- Recent diagnosis of Ulcerative Colitis within the last 12 months
- Ability to provide written informed consent
- Ability to comply with scheduled study procedures
You will not qualify if you...
- Younger than 18 years old
- Known active gastrointestinal disorders such as infectious gastroenteritis, celiac disease, Crohn disease, irritable bowel syndrome, chronic pancreatitis, or biliary salt diarrhea
- Previous colorectal surgery or presence of a cutaneous stoma
- Current or recent (within 2 weeks) therapy with drugs that may alter gut microbiota, including antimicrobials, probiotics, proton pump inhibitors, or metformin
- Decompensated heart failure or heart disease with ejection fraction below 30%
- Severe respiratory insufficiency
- Psychiatric disorders
- Pregnancy or breastfeeding
- Unable to provide informed consent
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
Gianluca Ianiro
Rome, Lazio, Italy, 00168
Actively Recruiting
Research Team
G
Gianluca Ianiro, MD
CONTACT
S
Serena Porcari, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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