Fecal Microbiota Transplantation for Treatment of Gastrointestinal Dysbiosis Clearance of ARO (FMTGID)
Primary Purpose
Dysbiosis, Antimicrobial Resistant Organism
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Fecal Microbiota Transplantation
Sponsored by
About this trial
This is an interventional treatment trial for Dysbiosis
Eligibility Criteria
Inclusion Criteria:
- Age 18 years or older.
- Able to provide informed consent.
- Willing and able to comply with all the required study procedures.
- Rectally colonized with antimicrobial resistant organisms: Extended-spectrum of beta-lactamase, Carbapenem resistant, vancomycin resistant enterococci
Exclusion Criteria:
- Planned or actively taking another investigational product
- Patients with neutropenia with absolute neutrophil count <0.5 x 109/L
- Evidence of toxic megacolon or gastrointestinal perforation on abdominal x-ray
- Peripheral white blood cell count > 30.0 x 109/L AND temperature > 38.0 ºC
- Active gastroenteritis due to Salmonella, Shigella, E. coli 0157H7, Yersinia or Campylobacter.
- Unable to tolerate FMT or enema for any reason.
- Requiring systemic antibiotic therapy at the time of FMT.
- Actively taking Saccharomyces boulardii or other probiotic; yogurt is allowed
- Severe underlying disease such that the patient is not expected to survive for at least 30 days.
- History of severe allergy to any food
Sites / Locations
- Vancouver Island Health Authority
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Open Label
Arm Description
Fecal Microbiota Transplantation
Outcomes
Primary Outcome Measures
Treatment
Symptom improvement in formal diagnosis of dysbiosis or clearance of antimicrobial resistant organism
Secondary Outcome Measures
Full Information
NCT ID
NCT03834051
First Posted
February 6, 2019
Last Updated
January 23, 2020
Sponsor
Vancouver Island Health Authority
1. Study Identification
Unique Protocol Identification Number
NCT03834051
Brief Title
Fecal Microbiota Transplantation for Treatment of Gastrointestinal Dysbiosis Clearance of ARO
Acronym
FMTGID
Official Title
Prospective, Open-label Trial to Evaluate Efficacy of Fecal Microbiota Transplantation for Treatment of Chronic Gastrointestinal Dysbiosis or Clearance of Antimicrobial Resistant Organism.
Study Type
Interventional
2. Study Status
Record Verification Date
January 2020
Overall Recruitment Status
Unknown status
Study Start Date
February 1, 2019 (Actual)
Primary Completion Date
August 2020 (Anticipated)
Study Completion Date
August 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Vancouver Island Health Authority
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The objective of this study is to assess the efficacy of FMTs via enema for 1) symptom improvement in individuals with a formal diagnosis of dysbiosis due to active inflammatory bowel disease or irritable bowel syndrome; 2) clearance of antimicrobial resistant organism from the gastrointestinal tract.
Detailed Description
Since the formal implementation of fecal microbiota transplantation trials at St. Joseph's Healthcare Hamilton in 2012, there are daily phone calls and e-mails from patients with a variety of chronic gastrointestinal disorders such as ulcerative colitis, Crohns, chronic irritable bowel syndrome, chronic severe constipation due to dysbiosis, which are formally diagnosed by gastroenterologists who specialize in this disorder to request for FMT. Out of desperation, some of these patients have explored the option of performing FMT at home.
There are instructions on how to manufacture and perform home FMTs on the internet. Given this some patients may perform FMTs at home using stool samples from unscreened and/or inappropriate donors. Individuals with metabolic disorders, family history of colonic cancer, autoimmune disease, gastrointestinal disorders as well as the ones whose blood and stools are unscreened should be excluded from donating stools. Unsupervised and using stool samples from an unscreened or unsuitable donor can lead to undesirable immediate and long-term consequences. The real possibility of these patients performing FMTs at home using stool samples from unscreened donors is very concerning.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dysbiosis, Antimicrobial Resistant Organism
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Open Label
Arm Type
Experimental
Arm Description
Fecal Microbiota Transplantation
Intervention Type
Drug
Intervention Name(s)
Fecal Microbiota Transplantation
Intervention Description
Fecal Microbiota Transplantation Enema Open Label
Primary Outcome Measure Information:
Title
Treatment
Description
Symptom improvement in formal diagnosis of dysbiosis or clearance of antimicrobial resistant organism
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 18 years or older.
Able to provide informed consent.
Willing and able to comply with all the required study procedures.
Rectally colonized with antimicrobial resistant organisms: Extended-spectrum of beta-lactamase, Carbapenem resistant, vancomycin resistant enterococci
Exclusion Criteria:
Planned or actively taking another investigational product
Patients with neutropenia with absolute neutrophil count <0.5 x 109/L
Evidence of toxic megacolon or gastrointestinal perforation on abdominal x-ray
Peripheral white blood cell count > 30.0 x 109/L AND temperature > 38.0 ºC
Active gastroenteritis due to Salmonella, Shigella, E. coli 0157H7, Yersinia or Campylobacter.
Unable to tolerate FMT or enema for any reason.
Requiring systemic antibiotic therapy at the time of FMT.
Actively taking Saccharomyces boulardii or other probiotic; yogurt is allowed
Severe underlying disease such that the patient is not expected to survive for at least 30 days.
History of severe allergy to any food
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine Lee
Organizational Affiliation
Vancouver Island Health Authority
Official's Role
Principal Investigator
Facility Information:
Facility Name
Vancouver Island Health Authority
City
Victoria
State/Province
British Columbia
ZIP/Postal Code
V8R 1J8
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Fecal Microbiota Transplantation for Treatment of Gastrointestinal Dysbiosis Clearance of ARO
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