search
Back to results

FMT in Ulcerative Colitis-Associated Pouchitis

Primary Purpose

Ulcerative Colitis Associated Pouchitis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
biologically active human fecal microbiota
sigmoidoscopy
Sponsored by
Virginia O. Shaffer
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis Associated Pouchitis focused on measuring ulcerative colitis, fecal microbiota transplantation

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • male or female
  • age 18 to 65 years
  • ulcerative colitis-associated pouchitis
  • patients of Emory Clinic and/or Emory University Hospital

Exclusion Criteria:

  • Age <18 years or >65 years of age
  • Exposure to immunosuppressive therapy (defined as steroid, etanercept, or anti-tumor necrosis factor (TNF)agents) within 1 month prior to enrollment
  • Concomitant Clostridium difficile infection
  • Suspected Crohn's disease
  • Documented active infection of any kind
  • Patients on anti-coagulant therapy, with platelet count less than 50,000, significant anemia with hemoglobin less than 7 or those with other conditions that place them at increased risk of bleeding
  • Absolute neutrophil count (ANC) less than 1000 or history of opportunistic infection
  • Administration of investigational drug within one month prior to planned FMT
  • Pregnant or breastfeeding women

Sites / Locations

  • Emory University
  • Emory St. Joseph's Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

fecal microbiota transplant

Arm Description

fecal microbiota transplant

Outcomes

Primary Outcome Measures

Number of Patients Who Experienced Improvement of Pouchitis Symptoms
Improvement of clinical pouchitis symptoms based on the clinical component of the modified pouchitis disease activity index (mPDAI) without relapse. These components include: stool frequency (number of stools), rectal bleeding, fecal urgency or abdominal cramps, or fever (temperature >37.8C).

Secondary Outcome Measures

Number of Patients With Favorable Microbiota Profile
16s ribosomal gene sequencing and metabolomic profile of the gut microbiota

Full Information

First Posted
January 27, 2014
Last Updated
March 18, 2019
Sponsor
Virginia O. Shaffer
search

1. Study Identification

Unique Protocol Identification Number
NCT02049502
Brief Title
FMT in Ulcerative Colitis-Associated Pouchitis
Official Title
The Use of Fecal Microbiota Transplantation in Patients With Ulcerative Colitis-associated Pouchitis
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
July 2014 (undefined)
Primary Completion Date
February 1, 2018 (Actual)
Study Completion Date
February 1, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Virginia O. Shaffer

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to test whether Fecal Microbiota Transplant (FMT) is a safe and effective treatment for people who have Ulcerative Colitis and have had an ileal pouch anastomosis. Ulcerative colitis (UC) is a type of inflammatory bowel disease (IBD) that may be caused by a person's immune system responding in an unusual way to bacteria normally found in the gut. Studies have shown that the gut bacteria in people with ulcerative colitis (UC) are different from the gut bacteria in people without ulcerative colitis (UC). Often, people with ulcerative colitis (UC) have fewer types of bacteria in their gut which can change the way that person's immune system works. This study is for people who have had a proctocolectomy with an ileal pouch anastomosis (IPAA) to treat ulcerative colitis (UC). More than 50% of people who have had an IPAA will develop a condition called pouchitis. Pouchitis is short or long-term inflammation of the ileal pouch that was created in order to store waste from your intestines. Patients with pouchitis are being asked to take part in this study. Currently, antibiotics, probiotics and prebiotics are used to treat pouchitis. However, it has been shown that probiotics are not very helpful once the patient stops taking them. In addition, antibiotics may cause unfavorable side effects. Fecal microbiota transplantation (FMT) is being studied as another form of treatment for patients with active pouchitis. Fecal microbiota transplantation (FMT) or "stool transplant" involves receiving a single fecal enema from someone who has volunteered to donate their stool. There are two purposes of this research study: To see whether or not fecal microbiota transplantation (FMT) is a useful treatment for patients with ulcerative colitis (UC) associated pouchitis To study the changes within the bacteria in the gut in patients with pouchitis (before and after study treatment) using stool, blood and urine samples

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis Associated Pouchitis
Keywords
ulcerative colitis, fecal microbiota transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Actual)

8. Arms, Groups, and Interventions

Arm Title
fecal microbiota transplant
Arm Type
Experimental
Arm Description
fecal microbiota transplant
Intervention Type
Biological
Intervention Name(s)
biologically active human fecal microbiota
Intervention Description
instillation of biologically active human fecal microbiota material via flexible sigmoidoscopy
Intervention Type
Procedure
Intervention Name(s)
sigmoidoscopy
Primary Outcome Measure Information:
Title
Number of Patients Who Experienced Improvement of Pouchitis Symptoms
Description
Improvement of clinical pouchitis symptoms based on the clinical component of the modified pouchitis disease activity index (mPDAI) without relapse. These components include: stool frequency (number of stools), rectal bleeding, fecal urgency or abdominal cramps, or fever (temperature >37.8C).
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Number of Patients With Favorable Microbiota Profile
Description
16s ribosomal gene sequencing and metabolomic profile of the gut microbiota
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: male or female age 18 to 65 years ulcerative colitis-associated pouchitis patients of Emory Clinic and/or Emory University Hospital Exclusion Criteria: Age <18 years or >65 years of age Exposure to immunosuppressive therapy (defined as steroid, etanercept, or anti-tumor necrosis factor (TNF)agents) within 1 month prior to enrollment Concomitant Clostridium difficile infection Suspected Crohn's disease Documented active infection of any kind Patients on anti-coagulant therapy, with platelet count less than 50,000, significant anemia with hemoglobin less than 7 or those with other conditions that place them at increased risk of bleeding Absolute neutrophil count (ANC) less than 1000 or history of opportunistic infection Administration of investigational drug within one month prior to planned FMT Pregnant or breastfeeding women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginia O. Shaffer, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emory University
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
Emory St. Joseph's Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30342
Country
United States

12. IPD Sharing Statement

Learn more about this trial

FMT in Ulcerative Colitis-Associated Pouchitis

We'll reach out to this number within 24 hrs