Long-term Efficacy and Safety of Fecal Microbiota Transplantation in Patients With Ulcerative Colitis
NCT ID: NCT07154784
Last Updated: 2025-09-12
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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ENROLLING_BY_INVITATION
PHASE2/PHASE3
30 participants
INTERVENTIONAL
2023-07-19
2027-06-30
Brief Summary
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Detailed Description
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In 2013, a landmark study published in the New England Journal of Medicine demonstrated that fecal microbiota transplantation (FMT)-a procedure in which processed stool from a healthy donor is delivered into a patient's colon via colonoscopy-significantly reduced the recurrence of antibiotic-associated Clostridioides difficile infection. Since then, FMT has been actively studied, particularly for its therapeutic potential in ulcerative colitis, a subtype of IBD.
Randomized controlled trials have investigated various methods of FMT delivery in ulcerative colitis, including colonoscopy, sigmoidoscopy, and oral capsules. No significant differences in efficacy have been reported between endoscopic and oral routes. In a domestic study on multidrug-resistant organisms, oral capsules showed promising outcomes in restoring microbial balance when compared with endoscopy and nasogastric tube administration.
While FMT delivery methods in Western countries are evolving from inpatient colonoscopic administration to outpatient enema or capsule-based regimens, South Korea currently lacks clinical research infrastructure for FMT beyond case reports. Although a few cases of FMT in IBD patients have been documented, no center has conducted formal clinical trials.
Therefore, this study aims to evaluate the clinical efficacy and underlying mechanisms of FMT in Korean patients with IBD, especially those with ulcerative colitis. Through this investigation, we seek to clarify the long-term therapeutic potential and safety of fecal microbiota transplantation in this population.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Ulcerative colitis patient
This was a multicenter, prospective study that enrolled patients diagnosed with ulcerative colitis who were aged between 10 and 80 years and had been receiving treatment for at least 3 months. Eligible participants were required to meet all of the following inclusion criteria:
1. age between 10 and 80 years;
2. a disease duration of ulcerative colitis of at least 3 months;
3. mild to moderate disease activity, defined by a Mayo score of 4-10 or a partial Mayo score of 2-7;
4. endoscopic evidence of rectal involvement extending ≥5 cm; and
5. willingness to provide written informed consent for participation in the study.
Fecal microbiota transplantation (FMT)
Fecal microbiota transplantation (FMT) will be performed at weeks 0 and 4 of study enrollment by administering approximately 250-300 cc of a multi-donor fecal suspension into the colon via sigmoidoscopy, colonoscopy, or by oral administration of an equivalent amount (4 capsules).
Interventions
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Fecal microbiota transplantation (FMT)
Fecal microbiota transplantation (FMT) will be performed at weeks 0 and 4 of study enrollment by administering approximately 250-300 cc of a multi-donor fecal suspension into the colon via sigmoidoscopy, colonoscopy, or by oral administration of an equivalent amount (4 capsules).
Eligibility Criteria
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Inclusion Criteria
* History of ulcerative colitis for at least 3 months
* Mild to moderate ulcerative colitis with a Mayo score of 4-10 or a partial Mayo score of 2-7
* Endoscopic evidence of rectal involvement extending at least 5 cm
* Willingness to provide written informed consent for participation in this clinical trial
Exclusion Criteria
* Neutropenia (absolute neutrophil count \< 500)
* Pregnancy
* Infectious colitis not caused by Clostridioides difficile
* History of colectomy (excluding appendectomy)
* History of antibiotic use within the past 2 weeks
* Use of corticosteroids \> 20 mg within the past 4 weeks
* Current or planned use of biologics (e.g., anti-TNF-α antibodies, anti-α4β7 integrin monoclonal antibodies, JAK inhibitors, anti-IL-12/IL-23 antibodies)
* Major food allergy
* Indeterminate colitis
* Comorbid chronic diseases such as chronic liver disease, heart failure, or chronic obstructive pulmonary disease (COPD)
* Refusal to participate in the study
* Any other condition deemed inappropriate for study participation by the investigator
10 Years
80 Years
ALL
No
Sponsors
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Seoul National University Bundang Hospital
OTHER
Inha University Hospital
OTHER
Seoul National University Boramae Hospital
OTHER
Seoul National University Hospital
OTHER
Responsible Party
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KwangWoo Kim
Professor
Locations
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Seoul Metropolitan Government Seoul National University Boramae Medical Center, Seoul National University College of Medicine
Seoul, Dongjak-gu, South Korea
Countries
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Other Identifiers
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2021-0314
Identifier Type: -
Identifier Source: org_study_id
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