Rationale: Postantibiotic diarrhoea in critically ill patients is common, often prolonged and currently there is no effective treatment of it. Aim: To test safety and feasibility of faecal microbial transplantation in critically ill patients with postantibiotic diarhoea. Design: Prospective, single center, parallel group randomised controlled trial. Subjects: ICU patients (both general and burn ICU) who developed diarhea after a course of antibiotic therapy that is persistent for 24 hours and is not due to other causes. Patients with septic shock or approaching death will be excluded. Treatment in the intervention group: Faecal bacteriotherapy (FBT) delivered as enema (and repeated once in the subgroup of patients with C. dif. infection) of 350 ml of standardised mixed transplantate prepared from faeces of 7 healthy donors. Control group: Standard-of-care protocolised treatment of postantibiotic diarhea (which includes vancomycine 250 mg p.o. 6 hourly in the subgroup with C. dif. infection). Primary outcome: Percentage of patients with treatment failure at day 7 after randomisation, which is defined as treatment either not being delivered or not being effective. Secondary and exploratory outcomes: Influence of the intervention on colonic microbiome and metabolome, small bowel and colonic permeability, bacterial translocation and systemic inflammation response to procedure.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
36
Enema of 350 ml of standardised mixed transplantate prepared from faeces of 7 healthy donors.
standard-of-care protocolised treatment of postantibiotic diarhea
Kralovske Vinohrady University Hospital
Prague, Czechia
RECRUITINGFrantišek Duška
Prague, Česká Republika, Czechia
RECRUITINGTreatment failure
Difference of proportion of patients between intervention and control groups in whom the treatment failed. Failure is defined as treatment has either not been delivered or has not been effective to cure diarrhoea as per WHO definition
Time frame: 7 days after randomisation
Comparison of therapeutic efficacy
Difference of proportion of patients between intervention and control groups who are diarhoea-free (WHO definition)
Time frame: 7 days after randomisation
Systemic inflammation
Difference between intervention and control group in area under C-reactive protein plasma concentration curve
Time frame: 7 days after randomisation
Organ failures
Difference between intervention and control group in SOFA score curve
Time frame: 7 days after randomisation
Postprocedural bacteriaemia
Difference between intervention and control group in the percentage of positive blood cultures
Time frame: 3 hours after intervention
Mortality
Difference between intervention and control group in the absolute risk of death (intention-to-treat analysis)
Time frame: 28 day or hospital discharge, whichever occurs earlier
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