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NCT Number: NCT05257538

FMT in Initial CDI

The study explores fecal microbiota transfer via retention enema after the first clostridioides difficile episode.

Recruiting

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Key information

Age range

18 year–120 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Turku University hospital

Turku, Finland

Location status: Recruiting

Location contact

Teppo Stenholm

CONTACT

[email protected]

023130000

About this study

Clostridioides difficile infections (CDI) remain a significant burden for the patients and the society. According to the National Institute for Health and Welfare (THL), in 2018 there were 4324 CDIs in Finland. C. difficile typically affects patients whose gut microbiota is profoundly damaged by antibiotics. Standard therapy for CDI is antibiotic such as vancomycin. After the standard therapy gut microbiota remains damaged and vulnerable to C difficile reinfection arising from spores that survived the treatment. Early recurrence of CDI is commonly defined as relapse of symptoms and positive testing for fecal C difficile within three months after the previous episode. Recurrent CDI is reported in 10-30% of patients after initial treatment, with recurrence approaching 60% after the third episode.

Fecal microbiota transplantation (FMT) is currently the most effective treatment for recurrent CDI (rCDI), with efficacy of over 90%. Even though FMT is mostly administered endoscopically, it is considered a cost-effective way to treat rCDI patients. FMT is recommended after the second relapse, in other words, after the third antibiotic course for CDI. FMT is most effective in rCDI when administered via colonoscopy. However, colonoscopy is a costly and invasive procedure. The largest study exploring a simple and inexpensive retention enema FMT for rCDI showed a 62% clinical response following a single FMT, and 85% after the second. Baro et al. found that FMT via enema was the most cost-effective initial strategy for the management of second recurrence of community-onset CDI.

In the controlled FMT trials the adverse events have been similar with placebo. Also, the long term safety in up to four years follow up seems to be good. The patients treated with FMT seem to normalize their bowel symptoms faster compared to CDI patients treated with only antibiotics.

FMT reduces antibiotic resistance genes in gut microbiota and therefore has a theoretical potential to reduce infections caused by multi-resistant organisms.

A balanced gut microbiota is important in infection control and essential to normal bowel function. CDI is an indicator of damaged gut microbiota. After a course of antibiotics, the gut microbiota typically becomes less diverse for at least some months. It is not known whether the gut microbiota ever regains its former constitution after such a treatment. We hypothesize that planting a new microbial population soon after antibiotic treatment for CDI reduces the risk of recurrence as well as post-infectious functional bowel disorders.

FMT via colonoscopy is currently recommended after the third CDI (second relapse). Our study explores FMT via inexpensive and minimally invasive retention enema after the first CDI episode.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • >18 years
  • C. difficile PCR in feces positive and clinical symptoms of enteritis.
  • Full resolution of diarrhea during antibiotic treatment for C. difficile
  • No other ongoing antibacterial treatments.
  • No ongoing probiotics.
  • Signed informed consent.

Exclusion criteria

  • Pregnant
  • Ongoing need for antibacterial treatment
  • Life expectancy < 1 year
  • Prior C. difficile infection in preceding 3 months
  • Unable to provide written consent, due to dementia for example.
  • Fecal incontinence i.e. inability to retain enema.

Treatment and study plan

FMT

Other

Fecal microbiota transfer from a healthy and tested volunteer

Placebo enema

Other

colored water enema

Primary outcomes

  1. clostridioides difficile relapse rate

    Time frame: month 3

Secondary outcomes

  1. Resolution of gastrointestinal symptoms

    Time frame: month 3 and 1 year

    Primary symptoms of clostridioides difficile infection

  2. composition of fecal microbiota

    Time frame: month 3 and 1 year

    Characterization of fecal microbiome samples down to species level by polymerase chain reaction (PCR)

  3. Retention time, i.e. time from FMT to subsequent defecation

    Time frame: day 1

  4. Fecal microbiota transfer adverse events

    Time frame: within 1 year of administration

    possibly transferred infections, complications of administration etc

  5. Adherence to FMT

    Time frame: From recruitment until FMT administration. Up to 15 days

  6. Alterations in mood as measured by total score of BDI

    Time frame: month 3 and 1 year

    0 to >30 points with higher points meaning more severe depression

  7. Anxiety as measured by total score of GAD-7

    Time frame: month 3 and 1 year

    0 to 21 points with higher points meaning more severe anxiety

  8. Quality of life as measured by 15D instrument

    Time frame: month 3 and 1 year

  9. clostridioides difficile relapse rate

    Time frame: 1 year

Study contacts

Contact information is provided by the study sponsor or research team.

Teppo U Stenholm

CONTACT

[email protected]

023130000

Sponsors and collaborators

Lead sponsor

Turku University Hospital

Other Gov

Collaborators

  • Helsinki University Central Hospital
  • PaijatHame Central Hospital
  • Satakunta Central Hospital

Registry information

Official study title

Fecal Microbiota Transplantation in Initial Clostridioides Difficile Enteritis: a Randomized, Placebo-controlled Trial

Acronym: FinCDI

Important dates

Study start
2021
Primary completion
2027
Study completion
2028
First posted
Feb 25, 2022
Registry last updated
Apr 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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