Clostridioides difficile (CD) infection (CDI) is a global health threat with an urgent need for new treatment strategies. Faecal microbiota transplantation (FMT) is effective for recurrent Clostridioides difficile infection (CDI), and is currently recommended for multiple (three or more), recurrent CDI infections. The role of FMT earlier in the treatment hierarchy of CDI remains to be determined. In this randomized, double-blinded, placebo-controlled clinical trial, we compare FMT with placebo following standard antibiotic treatment for first or second Clostridioides difficile infection.
This is a parallel arm placebo-controlled clinical trial. We aim to include 84 adult patients with their first or second episode of Clostridioides difficile (formerly Clostridium difficile) infection. All patients receive vancomycin standard therapy. Patients are randomised in a 1:1 ratio to two treatments with capsules that contain either FMT+FMT or placebo+placebo. The primary outcome is absence of C difficile-associated disease 8 weeks after randomisation. Patients who have fulminant disease where it is deemed unethical to give placebo are offered open-label FMT. The primary outcome in patients with fulminant C difficile infection is 8 weeks mortality.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
42
Single donor, fecal microbiota transplantion (FMT) from healthy human donors.
Food coloring, water, glycerol
Aarhus University Hospital
Aarhus N, Denmark
Resolution of CD-associated diarrhea (CDAD) week 8
Measured as a combined clinical resolution or persistent diarrhea, but with negative CD test.
Time frame: 8 weeks following treatment
Mortality week 8
In the open-label arm for patients who cannot be randomized due to ethical reasons, the primary outcome is mortality.
Time frame: 8 weeks following treatment
Resolution of CD-associated diarrhea (CDAD) week 1
Measured as a combined clinical resolution or persistent diarrhea, but with negative CD test.
Time frame: 1 week following treatment
Negative CD toxin-test week 1
Faecal C difficile PCR test
Time frame: 1 week following treatment
Negative CD toxin-test week 8
Faecal C difficile PCR test
Time frame: 8 weeks following treatment
Mortality week 8
Date of death
Time frame: 8 weeks
Colectomy rate week 8
Date of colectomy
Time frame: 8 weeks
Health-related quality of life
EDQ5D-5L
Time frame: 8 weeks
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