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Fecal Microbiota Transplantation for C Diff Infection

Primary Purpose

Clostridium Difficile Infection

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Human fecal matter
Sponsored by
Englewood Hospital and Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Clostridium Difficile Infection focused on measuring C diff, CDI, clostridium difficile associated diarrhea

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Subject is at least 18 years old.
  2. Subject has recurrent or relapsing CDI defined as:

    • 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, fidaxomicin). OR
    • At least two episodes of severe CDI resulting in hospitalization and associated with significant morbidity. OR
    • Moderate CDI not responding to standard therapy (vancomycin) for at least a week. OR
    • Severe C. difficile infection with toxic megacolon, not responding to standard therapy or the use of IVIg.
  3. Subject is willing and able to provide informed consent.
  4. If a female of childbearing potential, subject has agreed to use an acceptable form of birth control for up to 4 weeks after FMT treatment.

Exclusion Criteria:

  1. Subject is pregnant.
  2. Subject is unable to comply with study requirements.

Sites / Locations

  • Englewood Hospital and Medical CenterRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

All patients

Arm Description

150-500 ml of human fecal matter

Outcomes

Primary Outcome Measures

CDI recurrence
Number of patients who did/did not experience relapse in the 8 weeks post FMT

Secondary Outcome Measures

Full Information

First Posted
July 19, 2013
Last Updated
August 16, 2021
Sponsor
Englewood Hospital and Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01905709
Brief Title
Fecal Microbiota Transplantation for C Diff Infection
Official Title
Fecal Microbiota Transplantation for the Treatment of Recurrent or Refractory Clostridium Difficile Infection (CDI)
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Recruiting
Study Start Date
July 2013 (undefined)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Englewood Hospital and Medical Center

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to provide treatment with Fecal Microbiota Transplantation (FMT) to patients with recurrent or refractory Clostridium difficile infection (CDI). It has been shown that good bacteria (like that found in the stool from a healthy donor) attack Clostridium difficile in multiple ways: they make substances that kill Clostridium difficile - and they attach to the surface of the colon lining, which prevents the Clostridium difficile toxin (poison) from attaching. FMT involves infusing a mixture of saline and stool from a healthy donor into the bowel of the patient with CDI during a colonoscopy. The method used to deliver the FMT will depend on individual characteristics of the subject and is at the discretion of the treating physician. FMT may be administered by the following methods. Colonoscopy: This method allows full endoscopic examination of the colon and exclusion of comorbid conditions (such as IBD, malignancy or microscopic colitis) which may have an impact on subject's treatment or response to therapy. Sigmoidoscopy: This method still allows infusion of the stool into a more proximal segment of the colon than an enema, but may not require sedation. This method may be beneficial in subjects who are elderly or multiparous and who may have difficulty retaining the material when given as enema. Sigmoidoscopic administration eliminates the additional risks associated with colonoscopy in subjects who may not have a clear indication for colonoscopy. Retention enema: This method may be preferable in younger subjects who have already had recent endoscopic evaluation, in subjects who prefer not to undergo endoscopy or in subjects with significant co morbidities and may not tolerate endoscopy. The physician will administer 300-500 mL of the fecal suspension in aliquots of 60 mL, through the colonoscope or sigmoidoscope or 150 mL via retention enema. In cases of colonoscopic delivery, the material will be delivered to the most proximal point of insertion. The subject is encouraged to retain stool for as long as possible.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Clostridium Difficile Infection
Keywords
C diff, CDI, clostridium difficile associated diarrhea

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
All patients
Arm Type
Experimental
Arm Description
150-500 ml of human fecal matter
Intervention Type
Biological
Intervention Name(s)
Human fecal matter
Other Intervention Name(s)
human stool
Primary Outcome Measure Information:
Title
CDI recurrence
Description
Number of patients who did/did not experience relapse in the 8 weeks post FMT
Time Frame
8 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject is at least 18 years old. Subject has recurrent or relapsing CDI defined as: 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, fidaxomicin). OR At least two episodes of severe CDI resulting in hospitalization and associated with significant morbidity. OR Moderate CDI not responding to standard therapy (vancomycin) for at least a week. OR Severe C. difficile infection with toxic megacolon, not responding to standard therapy or the use of IVIg. Subject is willing and able to provide informed consent. If a female of childbearing potential, subject has agreed to use an acceptable form of birth control for up to 4 weeks after FMT treatment. Exclusion Criteria: Subject is pregnant. Subject is unable to comply with study requirements.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marc Fiorillo, MD
Phone
201-945-6564
Email
fiorillomd@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Rosabel Cascina
Email
rosabel.cascina@ehmc.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marc Fiorillo, MD
Organizational Affiliation
Englewood Hospital and Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Englewood Hospital and Medical Center
City
Englewood
State/Province
New Jersey
ZIP/Postal Code
07631
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marc Fiorillo, MD
Phone
201-945-6564
Email
fiorillomd@gmail.com
First Name & Middle Initial & Last Name & Degree
Dara Herman
Email
dara.herman@ehmchealth.org
First Name & Middle Initial & Last Name & Degree
Marc Fiorillo, MD
First Name & Middle Initial & Last Name & Degree
Mtichell Spinnell, MD
First Name & Middle Initial & Last Name & Degree
Mark Sapienza, MD
First Name & Middle Initial & Last Name & Degree
Sandarsh Kancherla, MD
First Name & Middle Initial & Last Name & Degree
Irina Kaplounov, MD
First Name & Middle Initial & Last Name & Degree
Michael Meininger, MD

12. IPD Sharing Statement

Links:
URL
https://www.englewoodhealth.org/for-healthcare-professionals/clinical-research-center
Description
Related Info

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Fecal Microbiota Transplantation for C Diff Infection

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