Fecal Microbiota Transplant (FMT) for Relapsing C. Difficile Infection in Adults and Children Using a Frozen Inoculum
Primary Purpose
Clostridium Difficile Infection
Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Fecal Microbiota Transplant (FMT)
Sponsored by
About this trial
This is an interventional treatment trial for Clostridium Difficile Infection focused on measuring Fecal Microbiota Transplant, Clostridium difficile, Diarrhea
Eligibility Criteria
Inclusion Criteria:
Patients with recurrent or relapsing CDI defined as EITHER(13):
- At least three episodes of mild-to-moderate CDI and failure of a 6-8 week taper with vancomycin with or without an alternative antibiotic (e.g. rifaximin, nitazoxanide).
- At least two episodes of severe CDI resulting in hospitalization and associated with significant morbidity.
- Willingness to accept risk of unrelated donor stool
- Willingness to be randomized to NGT vs. colonoscopic delivery.
- Able to consent for self, or parental assent/child assent as age appropriate.
Exclusion Criteria:
- Anatomic contraindication to NGT
- Delayed gastric emptying syndrome
- Known chronic aspiration
- Contraindication to colonoscopy (ASA 4 or more)
- High risk of bacterial translocation (Immunosuppression, cirrhosis etc)
- Pregnant or breastfeeding women
- Acute unrelated infection or comorbid illness exaccerbation
Sites / Locations
- Massachusetts General Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Colonoscopy
Nasogastric Tube (NGT)
Arm Description
Fecal microbiota transplant ("stool transplant") from healthy, unrelated donor via colonoscopy
Fecal microbiota transplant ("stool transplant") from healthy, unrelated donor via NGT
Outcomes
Primary Outcome Measures
Safety
Safety is assessed by clinical symptoms, exam, signs (GI and systemic)
Secondary Outcome Measures
Efficacy
Efficacy is defined as resolution of C. Difficile signs and symptoms off antibiotics for C. difficile
Full Information
NCT ID
NCT01704937
First Posted
October 4, 2012
Last Updated
June 18, 2014
Sponsor
Massachusetts General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT01704937
Brief Title
Fecal Microbiota Transplant (FMT) for Relapsing C. Difficile Infection in Adults and Children Using a Frozen Inoculum
Official Title
Fecal Microbiota Transplant (FMT) for Relapsing C. Difficile Infection in Adults and Children Using a Frozen Inoculum
Study Type
Interventional
2. Study Status
Record Verification Date
June 2014
Overall Recruitment Status
Completed
Study Start Date
November 2012 (undefined)
Primary Completion Date
May 2014 (Actual)
Study Completion Date
May 2014 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Fecal microbiota transplantation (FMT) is the reconstitution of normal flora by a "stool transplant" from a healthy individual to a C. difficile-infected recipient, and has long been a successful approach to recurrent/refractory C. difficile. The purpose of this project is to generate a frozen FMT inoculum from well-screened healthy volunteer donors which can be used repeatedly, particularly in those who do not have a healthy intimate partner or other related donor. Delivery of FMT has been performed colonoscopically, by fecal retention enema, or by the nasogastric route. This study will evaluate the safety and secondarily the efficacy of a frozen inoculum administered by nasogastric tube vs administered by colonoscope.
Subjects with recurrent/relapsing C. difficile infection (10 per group) will receive FMT via either:
colonoscopy
NGT
The primary endpoint is assessment of safety as measured by clinical events (GI, procedural, systemic). Efficacy will be defined as a resolution of diarrhea off antibiotics for C. difficile, in the absence of a need for OTHER systemic antibiotics, i.e. resumption of a normal bowel status for the individual. Secondary efficacy endpoints include weight, subjective well-being and relative clinical improvement per standardized questionnaire, and subject qualitative assessment of, and satisfaction with, the transplant procedures. Subjects will be monitored for clinical safety by history and standard exams and the follow-up questionnaire as well as followed closely by phone and in person.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clostridium Difficile Infection
Keywords
Fecal Microbiota Transplant, Clostridium difficile, Diarrhea
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
20 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Colonoscopy
Arm Type
Experimental
Arm Description
Fecal microbiota transplant ("stool transplant") from healthy, unrelated donor via colonoscopy
Arm Title
Nasogastric Tube (NGT)
Arm Type
Experimental
Arm Description
Fecal microbiota transplant ("stool transplant") from healthy, unrelated donor via NGT
Intervention Type
Drug
Intervention Name(s)
Fecal Microbiota Transplant (FMT)
Intervention Description
Reconstitution of normal flora by a "stool transplant" from a healthy individual to a C. difficile - infected recipient via colonoscopy or nasogastric tube
Primary Outcome Measure Information:
Title
Safety
Description
Safety is assessed by clinical symptoms, exam, signs (GI and systemic)
Time Frame
up to 6 mo post FMT
Secondary Outcome Measure Information:
Title
Efficacy
Description
Efficacy is defined as resolution of C. Difficile signs and symptoms off antibiotics for C. difficile
Time Frame
3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with recurrent or relapsing CDI defined as EITHER(13):
At least three episodes of mild-to-moderate CDI and failure of a 6-8 week taper with vancomycin with or without an alternative antibiotic (e.g. rifaximin, nitazoxanide).
At least two episodes of severe CDI resulting in hospitalization and associated with significant morbidity.
Willingness to accept risk of unrelated donor stool
Willingness to be randomized to NGT vs. colonoscopic delivery.
Able to consent for self, or parental assent/child assent as age appropriate.
Exclusion Criteria:
Anatomic contraindication to NGT
Delayed gastric emptying syndrome
Known chronic aspiration
Contraindication to colonoscopy (ASA 4 or more)
High risk of bacterial translocation (Immunosuppression, cirrhosis etc)
Pregnant or breastfeeding women
Acute unrelated infection or comorbid illness exaccerbation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elizabeth L Hohmann, MD
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
24762631
Citation
Youngster I, Sauk J, Pindar C, Wilson RG, Kaplan JL, Smith MB, Alm EJ, Gevers D, Russell GH, Hohmann EL. Fecal microbiota transplant for relapsing Clostridium difficile infection using a frozen inoculum from unrelated donors: a randomized, open-label, controlled pilot study. Clin Infect Dis. 2014 Jun;58(11):1515-22. doi: 10.1093/cid/ciu135. Epub 2014 Apr 23.
Results Reference
result
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Fecal Microbiota Transplant (FMT) for Relapsing C. Difficile Infection in Adults and Children Using a Frozen Inoculum
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