Fecal Microbiota Transplantation for Severe Clostridium Difficile Infection
Primary Purpose
Clostridium Difficile, Pseudomembranous Colitis
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Single-infusion FMT
Vancomycin (before randomization)
multiple-infusion FMT
Sponsored by
About this trial
This is an interventional treatment trial for Clostridium Difficile focused on measuring fecal microbiota transplantation, Clostridium difficile infection, pseudomembranous colitis
Eligibility Criteria
Inclusion criteria:
- Recurrent C. difficile infection (identified by positivity of C. difficile toxin in stools) with severe clinical picture (defined by the ESCMID Guidelines published in 2014 - Debast et al, Clin Microbiol Infect 2014)
- Possibility to undergo standard antimicrobial therapy for recurrent C. difficile infection Approval of informed consent
- Possibility to undergo protocol diagnostic and therapeutic procedures
- Stool negativity for parasites
- Stool negativity for Salmonella spp., Shigella spp., Yersinia enterocolitica, Campylobacter, Streptococcus agalactiae, Staphylococcus aureus, enteropathogenic Escherichia coli and other microorganisms except for C. difficile
- Blood negativity for: Hepatitis A virus-Immunoglobulin M, HBsAg, Anti-Hepatitis C Virus, Anti-Human Immunodeficiency Virus1-2, venereal disease reaction level (VDRL).
Exclusion Criteria:
- Subjects <18 years old
- Prior colectomy
- Negativity of C. difficile toxin in stools
- Mild clinical picture of C. difficile infection
- High risk of post-colonoscopy complications
- Other main gastrointestinal diseases (es. Crohn's disease or ulcerative colitis)
- Stool positivity for parasites
- Stool positivity for Salmonella spp., Shigella spp., Yersinia enterocolitica, Campylobacter, Streptococcus agalactiae, Staphylococcus aureus, enteropathogenic Escherichia coli and other microorganisms except for C. difficile
- Blood positivity for: Hepatitis A virus-Immunoglobulin M, HBsAg, Anti-Hepatitis C Virus, Anti-Human Immunodeficiency Virus1-2, venereal disease reaction level (VDRL).
- Pregnancy or breastfeeding.
- Inability to follow protocol procedures
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Multiple-infusion FMT
Single-infusion FMT
Arm Description
Repeated fecal infusions by colonoscopy. Before FMT, vancomycin is administered in all patients for 3 days
Single fecal infusion by colonoscopy.Before FMT, vancomycin is administered in all patients for 3 days
Outcomes
Primary Outcome Measures
Cure of C. difficile infection
Disappearance of C. difficile-associated diarrhea
Secondary Outcome Measures
Full Information
NCT ID
NCT03427229
First Posted
November 8, 2017
Last Updated
February 2, 2018
Sponsor
Catholic University of the Sacred Heart
1. Study Identification
Unique Protocol Identification Number
NCT03427229
Brief Title
Fecal Microbiota Transplantation for Severe Clostridium Difficile Infection
Official Title
Randomized Clinical Trial: Single Versus Multiple-infusion Fecal Microbiota Transplantation for Severe Clostridium Difficile Infection
Study Type
Interventional
2. Study Status
Record Verification Date
February 2018
Overall Recruitment Status
Completed
Study Start Date
March 2016 (Actual)
Primary Completion Date
October 30, 2017 (Actual)
Study Completion Date
October 30, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Catholic University of the Sacred Heart
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
Fecal microbiota transplantation (FMT) is acknowledged as a highly effective treatment for recurrent Clostridium difficile infection (CDI). Usually single fecal infusion achieves satisfactory cure rates of recurrent CDI). However, several retrospective studies show that severe clinical picture of recurrent CDI is a risk factor for the failure of single-infusion FMT, suggesting that multiple fecal infusions are required to cure this condition.
This is an open-label randomized clinical trial aiming to assess if multiple-infusion FMT is more effective than single-infusion FMT in curing severe CDI
Detailed Description
Fecal microbiota transplantation (FMT) is acknowledged as a highly effective treatment for recurrent Clostridium difficile infection (CDI). Usually single fecal infusion achieves satisfactory cure rates of recurrent CDI). However, several retrospective studies show that severe clinical picture of recurrent CDI is a risk factor for the failure of single-infusion FMT, suggesting that multiple fecal infusions are required to cure this condition.
This is an open-label randomized clinical trial aiming to assess if multiple-infusion FMT is more effective than single-infusion FMT in curing severe CDI
The investigators' study is an open-label randomized controlled trial, enrolling patients with recurrent and refractory C. difficile infection with a severe clinical picture of the disease.
At enrollment, C. difficile infection is defined as diarrhoea (at least 3 loose or watery stools per day for 2 or more consecutive days, or at least 8 loose stools in 48 hours) and positivity in the C. difficile toxin stool test.
Recurrent C. difficile infection is meant as the reappearance of clinical symptoms and positivity of C. difficile toxin test within 8 weeks after the end of the previous therapy.
Refractory CDI is defined as CDI unresponsive to the antimicrobial treatment, namely persistence of diarrhoea with CD toxin positive or persistent diarrhoea with toxin negative in the absence of other possible causes of diarrhoea (e.g. IBS, IBD, non-CDI antibiotic-associated diarrhea) Severe CDI is defined, according to the latest ESCMID guidelines, as: Episode of CDI with one or more specific clinical (fever, haemodynamic instability, respiratory failure which needs mechanical ventilation, signs and symptoms of peritonitis, signs and symptoms of colonic ileus), laboratory (marked leukocytosis, rise in serum creatinine and lactate, marked decrease of serum albumin), radiological (colon distension, colonic wall thickening) or endoscopic (pseudomembranous colitis), symptoms and signs of severe colitis or complicated course of disease.
Patients' stool are screened for detection of parasites and enteric bacterial pathogens to exclude other infective pathogens. Patients with former colectomy, inflammatory bowel diseases (IBD), irritable bowel syndrome (IBS), viral hepatitis, AIDS or syphilis will be excluded.
Patients are instructed and invited to signal recurrent symptoms and diarrhea after treatment. Monthly clinical and lab checks are performed for a period of 2 months after the treatment.
Treatment procedures:
All patients start therapy with vancomycin for 3 days before of stratification, with random allocation (1 to 1, through statistical software) to one of the two treatment schemes: 1) single-infusion FMT by colonoscopy, with the infusion in the cecum - through the biopsy channel - of 60-120 gr (depending on production) of donated feces, obtained from the donor within 6 hours from transplantation, and manually homogenized in 100/200 ml of physiological solution; colonoscopy will be performed by an expert endoscopist; preparation for colonoscopy (four liters of a solution with saline laxatives) will be provided 2) multiple-infusion FMT (with the same protocol of the other arm, but with repeated fecal infusions).
All patient will be instructed on hygiene rules to be followed at the patient's domicile to avoid re-infections at home. Stool donors will be selected following recommendations from the European FMT Working Group Consensus Conference.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clostridium Difficile, Pseudomembranous Colitis
Keywords
fecal microbiota transplantation, Clostridium difficile infection, pseudomembranous colitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
58 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Multiple-infusion FMT
Arm Type
Experimental
Arm Description
Repeated fecal infusions by colonoscopy. Before FMT, vancomycin is administered in all patients for 3 days
Arm Title
Single-infusion FMT
Arm Type
Active Comparator
Arm Description
Single fecal infusion by colonoscopy.Before FMT, vancomycin is administered in all patients for 3 days
Intervention Type
Biological
Intervention Name(s)
Single-infusion FMT
Intervention Description
Patients will receive a single fecal infusion by colonoscopy
Intervention Type
Drug
Intervention Name(s)
Vancomycin (before randomization)
Intervention Description
Vancomycin is administered in all patients for 3 days before randomization. Then vancomycin is stopped and patients are randomized to single-infusion FMT or multiple-infusion FMT.
Intervention Type
Biological
Intervention Name(s)
multiple-infusion FMT
Intervention Description
Patients will receive multiple fecal infusions by colonoscopy
Primary Outcome Measure Information:
Title
Cure of C. difficile infection
Description
Disappearance of C. difficile-associated diarrhea
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria:
Recurrent C. difficile infection (identified by positivity of C. difficile toxin in stools) with severe clinical picture (defined by the ESCMID Guidelines published in 2014 - Debast et al, Clin Microbiol Infect 2014)
Possibility to undergo standard antimicrobial therapy for recurrent C. difficile infection Approval of informed consent
Possibility to undergo protocol diagnostic and therapeutic procedures
Stool negativity for parasites
Stool negativity for Salmonella spp., Shigella spp., Yersinia enterocolitica, Campylobacter, Streptococcus agalactiae, Staphylococcus aureus, enteropathogenic Escherichia coli and other microorganisms except for C. difficile
Blood negativity for: Hepatitis A virus-Immunoglobulin M, HBsAg, Anti-Hepatitis C Virus, Anti-Human Immunodeficiency Virus1-2, venereal disease reaction level (VDRL).
Exclusion Criteria:
Subjects <18 years old
Prior colectomy
Negativity of C. difficile toxin in stools
Mild clinical picture of C. difficile infection
High risk of post-colonoscopy complications
Other main gastrointestinal diseases (es. Crohn's disease or ulcerative colitis)
Stool positivity for parasites
Stool positivity for Salmonella spp., Shigella spp., Yersinia enterocolitica, Campylobacter, Streptococcus agalactiae, Staphylococcus aureus, enteropathogenic Escherichia coli and other microorganisms except for C. difficile
Blood positivity for: Hepatitis A virus-Immunoglobulin M, HBsAg, Anti-Hepatitis C Virus, Anti-Human Immunodeficiency Virus1-2, venereal disease reaction level (VDRL).
Pregnancy or breastfeeding.
Inability to follow protocol procedures
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
29851107
Citation
Ianiro G, Masucci L, Quaranta G, Simonelli C, Lopetuso LR, Sanguinetti M, Gasbarrini A, Cammarota G. Randomised clinical trial: faecal microbiota transplantation by colonoscopy plus vancomycin for the treatment of severe refractory Clostridium difficile infection-single versus multiple infusions. Aliment Pharmacol Ther. 2018 Jul;48(2):152-159. doi: 10.1111/apt.14816. Epub 2018 May 30.
Results Reference
derived
Learn more about this trial
Fecal Microbiota Transplantation for Severe Clostridium Difficile Infection
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