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A Pilot Study of FMT on CD Patients With AIEC

Primary Purpose

Crohn Disease

Status
Active
Phase
Not Applicable
Locations
Hong Kong
Study Type
Interventional
Intervention
Fecal Microbiota Transplantation
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Crohn Disease focused on measuring Fecal Microbiota Transplant, Adherent-invasive Escherichia coli

Eligibility Criteria

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

Inclusion Criteria: >18 years of age; Patients with CD history ≥ 3-month duration; Patients with no or mild-to-moderate symptoms defined as Harvey Bradshaw Index (HBI) < 16 ; Patients with positive total E.coli antibodies (AEcAb) Exclusion Criteria: Pregnancy; New biological treatment or steroids use within 4 weeks; Current Colorectal tumor; Active gastrointestinal bleeding; Having ulcerative colitis; Having colectomy or partial colectomy (less than ileo-transverse colonic anastomosis); Having colonic or small bowel stoma; Active perianal lesions; Receiving antibiotics within 4 weeks; Presenting psychological or linguistic incapability to sign the informed consent

Sites / Locations

  • The Chinese University of Hong Kong

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Fecal Microbiota Transplantation

Arm Description

Recruited patients will receive Fecal Microbiota Transplantation

Outcomes

Primary Outcome Measures

Adverse Event
Occurrence of any adverse events

Secondary Outcome Measures

Change in AIEC colonization
Presence of mucosa-associated AIEC before and after receiving FMT
Change in inflammatory biomarker Erythrocyte sedimentation rate (ESR)
Change in inflammatory biomarker C-reactive protein (CRP)
Change in fecal microbiota
Fecal microbiota, including diversity, composition and functional capacity will be measured before and after receiving FMT
Disease Severity
Harvey Bradshaw Index score will be used to measure disease severity where scores higher than 16 indicate disease activity is severe

Full Information

First Posted
October 14, 2022
Last Updated
May 30, 2023
Sponsor
Chinese University of Hong Kong
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1. Study Identification

Unique Protocol Identification Number
NCT05611866
Brief Title
A Pilot Study of FMT on CD Patients With AIEC
Official Title
A Pilot Study of Fecal Microbiota Transplant (FMT) and Its Effects in Patients With Crohn's Disease With Moderate-to-High Risk of Colonization of Adherent-Invasive E. Coli (AIEC)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 12, 2022 (Actual)
Primary Completion Date
July 31, 2023 (Anticipated)
Study Completion Date
July 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

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 goal of this pilot study is to test whether Fecal Microbiota Transplant (FMT) would be an effective antibacterial treatment for managing Adherent-invasive Escherichia coli (AIEC) colonization in Crohn's disease (CD) patients. It aims to assess the safety of FMT in patients with clinically inactive or mild to moderate CD and to determine the presence of AIEC before and after FMT. Participants will receive FMT via colonoscopy and have a follow-up colonoscopy at the end of the study.
Detailed Description
Experimental and observational data suggest that intestinal inflammation in Crohn's Disease (CD) arises from abnormal immune response to intestinal microbiota in genetically susceptible individuals. Genes that regulate innate immune response, intestinal barrier function and bacteria killing of intracellular pathogens have been associated with an increased risk for developing CD in Caucasian populations. The search for specific pathogens in CD has identified in the intestinal mucosa of patients several candidates. One with much supporting evidence is the adherent invasive Escherichia coli (AIEC). Since its discovery in 1998, several groups have reported a higher prevalence of AIEC in CD patients compared to healthy subjects and confirmed their pro-inflammatory potential. A growing body of work indicates that different host environments can select such AIEC pathobiont. AIEC colonization in mice leads to strong inflammatory responses in the gut suggesting that AIEC could play a role in CD immunopathogenesis. Faecal microbiota transplantation (FMT) represents a clinically feasible way to restore the gut microbial ecology and has proven to be a breakthrough for the treatment of recurrent Clostridium difficile infection. Clinical trials are being conducted to evaluate its use for other conditions including inflammatory bowel disease, irritable bowel syndrome, diabetes mellitus, non-alcoholic steatohepatitis and hepatic encephalopathy. Efficacy of FMT on CD endoscopic lesions and AIEC colonization remains to be demonstrated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn Disease
Keywords
Fecal Microbiota Transplant, Adherent-invasive Escherichia coli

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All recruited patients will receive FMT.
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fecal Microbiota Transplantation
Arm Type
Experimental
Arm Description
Recruited patients will receive Fecal Microbiota Transplantation
Intervention Type
Procedure
Intervention Name(s)
Fecal Microbiota Transplantation
Intervention Description
FMT at Week 0
Primary Outcome Measure Information:
Title
Adverse Event
Description
Occurrence of any adverse events
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Change in AIEC colonization
Description
Presence of mucosa-associated AIEC before and after receiving FMT
Time Frame
Week 12
Title
Change in inflammatory biomarker Erythrocyte sedimentation rate (ESR)
Time Frame
Week 12
Title
Change in inflammatory biomarker C-reactive protein (CRP)
Time Frame
Week 12
Title
Change in fecal microbiota
Description
Fecal microbiota, including diversity, composition and functional capacity will be measured before and after receiving FMT
Time Frame
Week 12
Title
Disease Severity
Description
Harvey Bradshaw Index score will be used to measure disease severity where scores higher than 16 indicate disease activity is severe
Time Frame
Week 12

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: >18 years of age; Patients with CD history ≥ 3-month duration; Patients with no or mild-to-moderate symptoms defined as Harvey Bradshaw Index (HBI) < 16 ; Patients with positive total E.coli antibodies (AEcAb) Exclusion Criteria: Pregnancy; New biological treatment or steroids use within 4 weeks; Current Colorectal tumor; Active gastrointestinal bleeding; Having ulcerative colitis; Having colectomy or partial colectomy (less than ileo-transverse colonic anastomosis); Having colonic or small bowel stoma; Active perianal lesions; Receiving antibiotics within 4 weeks; Presenting psychological or linguistic incapability to sign the informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Siew Chien Ng, PhD
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Chinese University of Hong Kong
City
Sha Tin
ZIP/Postal Code
000000
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
No
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A Pilot Study of FMT on CD Patients With AIEC

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