Fecal microbiota transplantation (FMT) is a treatment that restores the balance of gut bacteria and is the most effective treatment for patients who suffer from recurrent Clostridioides difficile infection (CDI) brought on by antibiotic use. Although highly effective, we do not understand how FMT actually works. Freeze-dried or lyophilized fecal microbiota transplant (LFMT) has been shown to be effective. Recently, filtered fecal slurry, free of any live bacteria, has also been shown to cure 5 such patients. The advantage of the filtered fecal slurry is that it may be safer to patients as it does not contain any live bacteria. We have conducted a pilot study comparing LFMT to lyophilized sterile fecal filtrate (LSFF) in 9 patients, and found that the success rate of treatment was 80% vs 75% in these 2 groups. Therefore we need to perform a larger multicenter study to compare LFMT to LSFF to determine the success rate of curing these patients.
This prospective double blind randomized study will enroll 248 patients with recurrent Clostridium difficile infection (RCDI) in a 1:1 ratio to receive either LFMT or LSFF by capsules. Patients will receive 15 capsules at week 0 and be assessed at weeks 1, 4, 8 and 24. Blood, stool and urine samples will be collected. If the first treatment fails, patients will be given open label LFMT from the same donor. If treatment fails again, FMT will be offered in the form and route at the treating physician's discretion.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
138
15 capsules
15 capsules
University of Alberta Hospital
Edmonton, Alberta, Canada
University of British Columbia
Vancouver, British Columbia, Canada
University of British Columbia
Victoria, British Columbia, Canada
Mcgill University Health Centre
Montreal, Quebec, Canada
University Of Calgary
Calgary, Canada
Resolution of RCDI
Proportion of patients without RCDI
Time frame: 8 weeks
Resolution of RCDI
Proportion of patients with sustained cure
Time frame: 24 weeks
Serious Adverse Events
Mortality directly attributable to CDI or treatment
Time frame: 8 weeks
Serious Adverse Events
Infection directly attributable to treatment
Time frame: 8 weeks
Minor Adverse Events
Nausea
Time frame: 1 week
Minor Adverse Events
Vomiting
Time frame: 1 week
Minor Adverse Events
Abdominal discomfort
Time frame: 1 week
Difficulty swallowing capsules
Reported by patients as ranging between none, moderate or severe
Time frame: 1 week
Fever
Temperature of \>37.8C
Time frame: 1 week
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