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NCT06591013Completed

Efficacy and Mechanism of Fecal Microbiota Transplantation of the Bai Ethnicity in the Treatment of UC

Research on the Mechanisms of Different Donors in Fecal Microbiota Transplantation for Treating Ulcerative Colitis

Source: ClinicalTrials.gov · Last updated 30 Jun 2026

Brief summary (registry, in English)

Inflammatory bowel disease (IBD), including ulcerative colitis (UC) and Crohn's disease (CD), affects over 2 million people worldwide . Although biological therapies have significantly improved the treatment outcomes for UC, nearly two-thirds of patients experience diminishing drug responses over time, making it crucial to explore novel therapeutic approaches targeting the underlying pathophysiology of UC. UC is associated with alterations in gut microbiota, reduced microbial diversity, and changes in the relative abundance of dominant bacterial populations. Specifically, UC patients exhibit a marked decrease in gut microbiota diversity at the species level, with a reduction in Firmicutes (e.g., Clostridium butyricum) and an increase in Actinobacteria, Proteobacteria (e.g., Escherichia coli), Enterobacteriaceae, Streptococcus, and Bacteroides . Given the association between gut microbiota alterations and IBD activity, several studies have proposed microbiota-based therapies, particularly fecal microbiota transplantation (FMT), as a treatment for UC.

Status (registry)
Completed
Study type
Interventional
Enrollment
102 (actual)
First submitted
17 Jul 2024
Start date
14 Oct 2024
Primary completion date
20 Oct 2025
Lead sponsor
First Affiliated Hospital of Kunming Medical University
NCT number
NCT06591013

What you commit to

  • Study type: Interventional
  • Participants enrolled: 102
  • From 14 Oct 2024 to the primary completion date, 20 Oct 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Steroid dependence requiring \>20 mg prednisone or \>9 mg budesonide daily at enrollment.
  • Recent or anticipated usage of prohibited drugs during the study period, including:
    • Rectal corticosteroids within 2 weeks prior to the first FMT.
    • Biologics (e.g., infliximab, adalimumab, vedolizumab) within 4 weeks prior to the first FMT.
    • Other major immunosuppressants (e.g., calcineurin inhibitors, antitumor drugs) within 12 weeks prior to treatment.
    • Probiotics within 4 weeks before the first FMT.
    • Experimental drugs or protocols within 12 weeks before the first FMT.
    • Anti-tuberculosis (TB or MAC) treatment within 4 weeks before the first FMT.
    • Permitted Medications:
    • Participants may continue using the following medications if doses are stable within specified timeframes before the first FMT:
  • Oral prednisone (≤20 mg/day, stable for 2 weeks, gradually tapered at a rate of 2.5 mg/week to discontinue by week 8).
    • Subjects should maintain the same doses of oral 5-aminosalicylates, thiopurines, and methotrexate during the study. For oral prednisolone, the dose had to be tapered off gradually, at a rate of 2.5mg per week, so that subjects were no longer exposed to steroids until week 8.
    • Prohibited Medications:
  • Rectal corticosteroids (2 weeks before and throughout the study).
  • Antibiotics, antifungals, antivirals, probiotics, or prebiotics (4 weeks before and throughout the study).
  • Biologics or calcineurin inhibitors (12 weeks before and throughout the study). Participants using prohibited medications during the study will remain enrolled, and outcomes will still be evaluated. All prohibited medication usage will be recorded.

Other illness

  • Evidence or history of toxic megacolon.
  • Diagnosed with Crohn's disease or indeterminate colitis.
  • Participants with perianal diseases (e.g., fistulae, anal fissures).
  • History of significant gastrointestinal surgery (e.g., colectomy) :
    • Minor surgeries will be reviewed case by case.
    • Patients with appendectomy within 3 months will be excluded.

Other

  • Participants unable to provide informed consent, answer questionnaires, or supply samples.
  • Pregnant women or those attempting to conceive.
  • Participants unwilling to use effective contraception throughout the study.
  • Participants deemed in remission by investigators.
  • Isolated rectal inflammation (\<5 cm in extent).
  • Antibiotic use within the past 4 weeks for any reason, including for UC.
  • Oral 5-aminosalicylic acid (stable for 4 weeks).
  • Azathioprine and methotrexate (≥90 days of use with stable doses for 4 weeks).

Who the study is looking for

  • Age between 14 and 79 years (inclusive), any gender.
  • Diagnosed with ulcerative colitis (UC) per established clinical, endoscopic, and histological standards, with a disease duration of over 3 months.
  • Active mild-to-moderate UC, defined by a Mayo score of 4-10, including an endoscopic score ≥1 and a physician's global assessment score ≤2.
  • Stable baseline medication consisting of 5-aminosalicylic acid (mesalamine).
  • Signed written informed consent.

Age in the registry: 14 years to 79 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
China
Coordinator of this site? Confirm its status
KunmingChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.