FMT in Initial CDI (FinCDI)
Primary Purpose
Clostridioides Difficile Infection
Status
Recruiting
Phase
Not Applicable
Locations
Finland
Study Type
Interventional
Intervention
FMT
placebo enema
Sponsored by
About this trial
This is an interventional treatment trial for Clostridioides Difficile Infection
Eligibility Criteria
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.
Sites / Locations
- Turku University hospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
FMT enema
plasebo enema
Arm Description
FMT enema 3-5 days after standard antibiotic treatment
placebo
Outcomes
Primary Outcome Measures
clostridioides difficile relapse rate
Secondary Outcome Measures
Resolution of gastrointestinal symptoms
Primary symptoms of clostridioides difficile infection
composition of fecal microbiota
Characterization of fecal microbiome samples down to species level by polymerase chain reaction (PCR)
Retention time, i.e. time from FMT to subsequent defecation
Fecal microbiota transfer adverse events
possibly transferred infections, complications of administration etc
Adherence to FMT
Alterations in mood as measured by total score of BDI
0 to >30 points with higher points meaning more severe depression
Anxiety as measured by total score of GAD-7
0 to 21 points with higher points meaning more severe anxiety
Quality of life as measured by 15D instrument
clostridioides difficile relapse rate
Full Information
NCT ID
NCT05257538
First Posted
January 27, 2022
Last Updated
April 11, 2023
Sponsor
Turku University Hospital
Collaborators
Helsinki University Central Hospital, Päijät Häme Central Hospital, Satakunta Central Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05257538
Brief Title
FMT in Initial CDI
Acronym
FinCDI
Official Title
Fecal Microbiota Transplantation in Initial Clostridioides Difficile Enteritis: a Randomized, Placebo-controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 1, 2021 (Actual)
Primary Completion Date
December 30, 2024 (Anticipated)
Study Completion Date
December 30, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Turku University Hospital
Collaborators
Helsinki University Central Hospital, Päijät Häme Central Hospital, Satakunta Central Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study explores fecal microbiota transfer via retention enema after the first clostridioides difficile episode.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clostridioides Difficile Infection
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
140 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
FMT enema
Arm Type
Active Comparator
Arm Description
FMT enema 3-5 days after standard antibiotic treatment
Arm Title
plasebo enema
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Other
Intervention Name(s)
FMT
Intervention Description
Fecal microbiota transfer from a healthy and tested volunteer
Intervention Type
Other
Intervention Name(s)
placebo enema
Intervention Description
colored water enema
Primary Outcome Measure Information:
Title
clostridioides difficile relapse rate
Time Frame
month 3
Secondary Outcome Measure Information:
Title
Resolution of gastrointestinal symptoms
Description
Primary symptoms of clostridioides difficile infection
Time Frame
month 3 and 1 year
Title
composition of fecal microbiota
Description
Characterization of fecal microbiome samples down to species level by polymerase chain reaction (PCR)
Time Frame
month 3 and 1 year
Title
Retention time, i.e. time from FMT to subsequent defecation
Time Frame
day 1
Title
Fecal microbiota transfer adverse events
Description
possibly transferred infections, complications of administration etc
Time Frame
within 1 year of administration
Title
Adherence to FMT
Time Frame
From recruitment until FMT administration. Up to 15 days
Title
Alterations in mood as measured by total score of BDI
Description
0 to >30 points with higher points meaning more severe depression
Time Frame
month 3 and 1 year
Title
Anxiety as measured by total score of GAD-7
Description
0 to 21 points with higher points meaning more severe anxiety
Time Frame
month 3 and 1 year
Title
Quality of life as measured by 15D instrument
Time Frame
month 3 and 1 year
Title
clostridioides difficile relapse rate
Time Frame
1 year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
120 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Teppo U Stenholm
Phone
023130000
Email
teppo.stenholm@tyks.fi
Facility Information:
Facility Name
Turku University hospital
City
Turku
Country
Finland
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Teppo Stenholm
Phone
023130000
Email
teppo.stenholm@tyks.fi
12. IPD Sharing Statement
Plan to Share IPD
No
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FMT in Initial CDI
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