Lyophilized Fecal Microbiota Transplantation for Recurrent Clostridium Difficile Infection
Primary Purpose
Clostridium Difficile Infection
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Lyophilized Fecal Microbiota Transplantation
Sponsored by
About this trial
This is an interventional treatment trial for Clostridium Difficile Infection
Eligibility Criteria
Inclusion Criteria:
- Age ≥ 12 years or older.
- Able to provide informed consent.
- Willing and able to comply with all the required study procedures.
- A positive stool test for C. difficile toxin/gene using either PCR or enzyme immunoassay within 3 months of recruitment unless patient taking treatment specifically for CDI for more than 3 months.
History of at least ≥ 2 recurrent CDI where recurrence is defined as return of diarrhea consistent with CDI within 8 weeks following CDI symptom resolution for at least 24 hours after a minimum of 10-day course of standard antibiotic therapy for each episode and/or ongoing symptoms consistent with CDI* (defined below) despite at least 7 days of treatment using oral vancomycin at a minimum dose of 250 mg four times daily.
- Symptoms of CDI include: diarrhea defined as: 3 or more unformed bowel movements in 24 hours for a minimum of 2 days with no other causes for diarrhea
Exclusion Criteria:
- Planned or actively taking another investigational product
- CDI symptom-free for 3 or more weeks following completion of CDI treatment
- Patients with neutropenia with absolute neutrophil count <0.5 x 109/L
- Evidence of toxic megacolon or gastrointestinal perforation on abdominal x-ray
- Active gastroenteritis due to Salmonella, Shigella, E. coli 0157H7, Yersinia or Campylobacter.
- Presence of colostomy
- Unable to tolerate FMT or enema for any reason.
- Requiring systemic antibiotic therapy for more than 7 days.
- 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.
Sites / Locations
- Vancouver Island Health Authority
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Open Label Lyophilized Fecal Microbiota Transplantation
Arm Description
Eligible participants with history of recurrent or refractory CDI
Outcomes
Primary Outcome Measures
Treatment of CDI
Evaluate treatment efficacy determined by no recurrence of CDI-related diarrhea
Secondary Outcome Measures
Full Information
NCT ID
NCT03834038
First Posted
February 6, 2019
Last Updated
May 15, 2019
Sponsor
Vancouver Island Health Authority
1. Study Identification
Unique Protocol Identification Number
NCT03834038
Brief Title
Lyophilized Fecal Microbiota Transplantation for Recurrent Clostridium Difficile Infection
Official Title
Prospective, Open-label Trial to Evaluate Efficacy of Lyophilized Fecal Microbiota Transplantation for Treatment of Recurrent C. Difficile Infection
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Unknown status
Study Start Date
February 18, 2016 (Actual)
Primary Completion Date
June 2019 (Anticipated)
Study Completion Date
March 2020 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
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 primary goal is to study participants with recurrent C. difficile infection (CDI) treated with lyophilized fecal microbiota transplantation (FMT). The safety, clinical response and relapse rate in patients will be assessed.
Detailed Description
Recurrence of CDI following a course of standard antibiotic therapy is high, especially in the elderly patients over 65 years of age, in hospitalized and in the immunocompromised patients. As CDI is characterized by intestinal dysbiosis. Fecal Microbiology Transplantation (FMT) has been investigated as alternative treatment for CDI and has been determined to be effective and safe. One of the major challenges of offering FMT is the availability of suitable donors. A donor may no longer be able to continue to donate for a number of reasons and this may lead to temporary interruption of FMT in centers which offer the program. In order to continue to offer FMT whenever needed, we will investigate the efficacy of lyophilized FMT. The lyophilization (freeze-drying) process works by dehydrating a frozen donor stool sample to complete dryness, using controlled temperature and pressure gradients. This lyophilized process results in a powdered form of the sample. Studies have shown that lyophilized donor stool samples have similar microbial compositions as the same fresh sample.The technique of freeze drying has been used for decades for the industrial storage of microbes and has been used. Preliminary study of lyophilized stool for FMT has been performed in dogs. Preliminary efficacy data in dogs with inflammatory bowel disease suggest equal efficacy as compared to fresh stool, although controlled study has yet to be performed. Should the lyophilized FMT (L-FMT) demonstrate to be equally or more effective than frozen FMT, there would be significant advantages. As with frozen FMT, lyophilized FMT will allow patients to receive FMT immediately as it can take up to two weeks for a donor's screening laboratory testing results to be available. Lyophilized FMT will also be more cost effective as less number of donors will need to be screened given the prolonged shelf life of lyophilized FMT which can be kept at above the freezing temperature. 9 This will also allow wider distribution and accessibility especially to the regions with limited capacity to manufacture FMT.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clostridium Difficile Infection
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Open Label Lyophilized Fecal Microbiota Transplantation
Arm Type
Experimental
Arm Description
Eligible participants with history of recurrent or refractory CDI
Intervention Type
Drug
Intervention Name(s)
Lyophilized Fecal Microbiota Transplantation
Intervention Description
Lyophilized FMT
Primary Outcome Measure Information:
Title
Treatment of CDI
Description
Evaluate treatment efficacy determined by no recurrence of CDI-related diarrhea
Time Frame
13 weeks from last FMT
10. Eligibility
Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥ 12 years or older.
Able to provide informed consent.
Willing and able to comply with all the required study procedures.
A positive stool test for C. difficile toxin/gene using either PCR or enzyme immunoassay within 3 months of recruitment unless patient taking treatment specifically for CDI for more than 3 months.
History of at least ≥ 2 recurrent CDI where recurrence is defined as return of diarrhea consistent with CDI within 8 weeks following CDI symptom resolution for at least 24 hours after a minimum of 10-day course of standard antibiotic therapy for each episode and/or ongoing symptoms consistent with CDI* (defined below) despite at least 7 days of treatment using oral vancomycin at a minimum dose of 250 mg four times daily.
Symptoms of CDI include: diarrhea defined as: 3 or more unformed bowel movements in 24 hours for a minimum of 2 days with no other causes for diarrhea
Exclusion Criteria:
Planned or actively taking another investigational product
CDI symptom-free for 3 or more weeks following completion of CDI treatment
Patients with neutropenia with absolute neutrophil count <0.5 x 109/L
Evidence of toxic megacolon or gastrointestinal perforation on abdominal x-ray
Active gastroenteritis due to Salmonella, Shigella, E. coli 0157H7, Yersinia or Campylobacter.
Presence of colostomy
Unable to tolerate FMT or enema for any reason.
Requiring systemic antibiotic therapy for more than 7 days.
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine Lee, MD
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
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Lyophilized Fecal Microbiota Transplantation for Recurrent Clostridium Difficile Infection
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