FMT for Moderate to Severe CDI: A Randomised Study With Concurrent Stool Microbiota Assessment
Primary Purpose
Clostridium Difficile Infection
Status
Active
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Fecal Microbiota Transplantation
Vancomycin
Sponsored by
About this trial
This is an interventional treatment trial for Clostridium Difficile Infection
Eligibility Criteria
Inclusion Criteria:
- C. difficile infection defined as diarrhea (≥3 soft, loose or watery stools per day for at least 2 consecutive days or ≥8 soft or loose stools in 48 hours) and a positive stool test for C. difficile toxin; and
- Age ≥ 18; and
- Written informed consent obtained
Exclusion Criteria:
- The presence of human immunodeficiency virus (HIV) infection with a CD4 count of less than 240
- Pregnancy
- GI Bleeding
- Acute coronary syndrome
Sites / Locations
- Prince of Wales Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Fecal Microbiota Transplantatio
Standard Therapy
Arm Description
Fecal Microbiota Transplantation of stool from healthy donor to recipient.
125mg Vancomycin four times per day
Outcomes
Primary Outcome Measures
Number of participants cured without relapse within 10 weeks after the initiation of therapy
Relapse is defined as diarrhea with a positive stool test for C. difficile toxin. An adjudication committee members who are not aware of the study-group assignment will make final decision on which patients are considered cured.
Secondary Outcome Measures
30-day mortality rate
mortality rate is measured.
30-day colectomy rates
Colectomy rates is measured.
Number of day of hospital stay
The total hospital day is measured.
Changes in the stool microbiota after FMT measured using pyrosequencing
We will do pyrosequencing using the study stool samples from patients and donors
Full Information
NCT ID
NCT02570477
First Posted
October 5, 2015
Last Updated
February 7, 2023
Sponsor
Chinese University of Hong Kong
1. Study Identification
Unique Protocol Identification Number
NCT02570477
Brief Title
FMT for Moderate to Severe CDI: A Randomised Study With Concurrent Stool Microbiota Assessment
Official Title
Fecal Microbiota Transplantation (FMT) for Moderate to Severe Clostridium Difficile Infection (CDI): A Randomised Study With Concurrent Stool Microbiota Assessment (FMT-CDI-RCT Study)
Study Type
Interventional
2. Study Status
Record Verification Date
February 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2015 (Actual)
Primary Completion Date
January 2018 (Actual)
Study Completion Date
December 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Clostridium difficile infection (CDI) is a leading cause of hospital-associated gastrointestinal illness, associated with significant morbidity and mortality and has a high burden on health-care system. The incidence of CDI has increased to epidemic proportion worldwide over the past decade. Community-acquired CDI, elderly and hospitalized patients receiving antibiotics are the main group at risk for developing CDI.
Currently, the first-line treatment for C. difficile-associated diarrhea includes cessation of the antibiotic implicated in the development of CDI, treatment with metronidazole or vancomycin and recently Fidaxomicin which is yet to be available in Hong Kong. However, disease recurrence is an increasing problem and 20% to 60% of patients experience at least one recurrence within a few weeks of completion of antibiotic treatment. Moreover, an increasing number of patients who require life-saving emergency colectomy experience persistent CDI after surgery. Until recently, an effective treatment against recurrent CDI is not available. Generally, repeated and extended courses of vancomycin are prescribed.
Fecal microbiota transplantation (FMT) defined as infusion of feces from healthy donors to affected subjects has attracted great interest in recent years and is now recommended as the most effective therapy for CDI not responding to standard therapies. Systematic reviews of prospective trials, case series and one randomized controlled trial have shown an overall cure rate of close to 100%. More than 50% of patients stated they would have FMT as their preferred first treatment option if CDI were to recur.
This proposal aims to investigate the efficacy of FMT as first line therapy in patients with severe CDI and to assess changes in the fecal microbiota after FMT using pyrosequencing techniques.
Detailed Description
Clostridium difficile infection (CDI) is a leading cause of hospital-associated gastrointestinal illness, associated with significant morbidity and mortality and has a high burden on health-care system. The incidence of CDI has increased to epidemic proportion worldwide over the past decade. Community-acquired CDI, elderly and hospitalized patients receiving antibiotics are the main group at risk for developing CDI 1.
Currently, the first-line treatment for C. difficile-associated diarrhea includes cessation of the antibiotic implicated in the development of CDI, treatment with metronidazole or vancomycin and recently Fidaxomicin which is yet to be available in Hong Kong2. However, disease recurrence is an increasing problem and 20% to 60% of patients experience at least one recurrence within a few weeks of completion of antibiotic treatment. Moreover, an increasing number of patients who require life-saving emergency colectomy experience persistent CDI after surgery. Until recently, an effective treatment against recurrent CDI is not available. Generally, repeated and extended courses of vancomycin are prescribed3.
Fecal microbiota transplantation (FMT) defined as infusion of feces from healthy donors to affected subjects has attracted great interest in recent years and is now recommended as the most effective therapy for CDI not responding to standard therapies 4. Systematic reviews of prospective trials, case series and one randomized controlled trial have shown an overall cure rate of close to 100% 5, 6. More than 50% of patients stated they would have FMT as their preferred first treatment option if CDI were to recur 7.
While FMT has been proven to be effective in refractory CDI, the role of FMT as first-line therapy in a subset of patients with severe CDI, or high risk features for severe CDI has not been studied. These are generally patients in whom the risk of colectomy and mortality is exceedingly high. In addition, the mechanism of FMT in CDI is not completely clear, and limited data are available on the effects of FMT on the microbiota post FMT. It has been suggested that CDI results in deficiencies in fecal flora composition, particularly of Bacteroides and Firmicutes, and these deficiencies in the microbiota facilitate colonization with C. difficile. Microarray analysis in small number of subjects has shown a major shift in the patients' microbiota after donor-feces infusion toward that of the donors8. The experimental tools required for in depth analysis of the intestinal microbiota are now becoming available. This study aims to investigate the efficacy of FMT as first line therapy in patients with moderate to severe CDI and to assess changes in the fecal microbiota after FMT using pyrosequencing techniques.
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
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Fecal Microbiota Transplantatio
Arm Type
Active Comparator
Arm Description
Fecal Microbiota Transplantation of stool from healthy donor to recipient.
Arm Title
Standard Therapy
Arm Type
Active Comparator
Arm Description
125mg Vancomycin four times per day
Intervention Type
Procedure
Intervention Name(s)
Fecal Microbiota Transplantation
Other Intervention Name(s)
FMT infusion
Intervention Description
Healthy donor is screened and donates feces. It will then be diluted with sterile saline, blended and filtered. Supernatant will be infused to recipient.
Intervention Type
Drug
Intervention Name(s)
Vancomycin
Intervention Description
125mg Vancomycin four times per day
Primary Outcome Measure Information:
Title
Number of participants cured without relapse within 10 weeks after the initiation of therapy
Description
Relapse is defined as diarrhea with a positive stool test for C. difficile toxin. An adjudication committee members who are not aware of the study-group assignment will make final decision on which patients are considered cured.
Time Frame
10 weeks
Secondary Outcome Measure Information:
Title
30-day mortality rate
Description
mortality rate is measured.
Time Frame
30 days
Title
30-day colectomy rates
Description
Colectomy rates is measured.
Time Frame
30 days
Title
Number of day of hospital stay
Description
The total hospital day is measured.
Time Frame
up to 30 days
Title
Changes in the stool microbiota after FMT measured using pyrosequencing
Description
We will do pyrosequencing using the study stool samples from patients and donors
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
C. difficile infection defined as diarrhea (≥3 soft, loose or watery stools per day for at least 2 consecutive days or ≥8 soft or loose stools in 48 hours) and a positive stool test for C. difficile toxin; and
Age ≥ 18; and
Written informed consent obtained
Exclusion Criteria:
The presence of human immunodeficiency virus (HIV) infection with a CD4 count of less than 240
Pregnancy
GI Bleeding
Acute coronary syndrome
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siew Chien Ng
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Prince of Wales Hospital
City
Hong Kong
Country
Hong Kong
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
28539351
Citation
Zuo T, Wong SH, Lam K, Lui R, Cheung K, Tang W, Ching JYL, Chan PKS, Chan MCW, Wu JCY, Chan FKL, Yu J, Sung JJY, Ng SC. Bacteriophage transfer during faecal microbiota transplantation in Clostridium difficile infection is associated with treatment outcome. Gut. 2018 Apr;67(4):634-643. doi: 10.1136/gutjnl-2017-313952. Epub 2017 May 24.
Results Reference
derived
Learn more about this trial
FMT for Moderate to Severe CDI: A Randomised Study With Concurrent Stool Microbiota Assessment
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