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Faecal Microbiota Transplantation From Normal Pouch Function Donor in the Treatment of Chronic Pouchitis

Primary Purpose

Pouchitis, Inflammatory Bowel Diseases, Ulcerative Colitis

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Faecal microbiota transplantation
Sponsored by
Ole Thorlacius-Ussing, MD, DMSc, Professor of Surgery
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pouchitis focused on measuring FMT, Microbiota

Eligibility Criteria

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

Inclusion Criteria:

  • Patients ≥ 18 years of age with a J-pouch
  • PDAI ≥ 7
  • Established diagnosis of chronic pouchitis (≥3 times of pouchitis within the last year, symptoms more than 4 weeks despite antibiotic treatment)
  • Antibiotic treatment for pouchitis (ciprofloxacin and/or metronidazole) within the 3 months

Exclusion Criteria:

  • Immunosuppression
  • Pregnancy or breastfeeding
  • Evidence of intestinal pathogen bacteria in the stool at inclusion visit
  • Any severe or newly diagnosed concomitant cardiovascular, hepatic, intestinal, renal, endocrine, pulmonary, dental disease with inflammation or psychiatric disorder, which, in the opinion of the investigator, might have an influence on the patient's compliance or the interpretation of the results
  • Probiotic intake within the last 2 weeks prior to study intervention
  • Participation in another clinical trial within the previous 30 days before baseline
  • Serious food allergies with earlier anaphylactic reactions

Sites / Locations

  • Department of Gastrointestinal Surgery, Aalborg University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FMT

Arm Description

Outcomes

Primary Outcome Measures

Number of patients achieving clinical remission assessed by PDAI
Clinical remission is defined as PDAI<7

Secondary Outcome Measures

Number of patients achieving clinical response assessed by PDAI
Clinical response is defined as reduction of PDAI score >2
Engraftment of the donor microbiota in the patients
Assessed by beta-diversity

Full Information

First Posted
March 25, 2021
Last Updated
July 12, 2022
Sponsor
Ole Thorlacius-Ussing, MD, DMSc, Professor of Surgery
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1. Study Identification

Unique Protocol Identification Number
NCT04820413
Brief Title
Faecal Microbiota Transplantation From Normal Pouch Function Donor in the Treatment of Chronic Pouchitis
Official Title
Faecal Microbiota Transplantation Using Stool From Normal Pouch Function Donor in the Treatment of Chronic Pouchitis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2022
Overall Recruitment Status
Completed
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
March 15, 2022 (Actual)
Study Completion Date
March 15, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Ole Thorlacius-Ussing, MD, DMSc, Professor of Surgery

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with chronic pouchitis is disabled by bloody diarrhoea and abdominal pain often followed by fever. Pouchitis is an inflammation in a pouch, a reservoir formed by the small intestine in the management of the chronic inflammatory bowel disease, ulcerative colitis. The standard treatment for pouchitis is intensive broad-spectrum antibiotics for a longer period. However, the treatment often fails after repeated treatments. Studies show that patients with pouchitis have an altered composition of the gut microbiota compared to healthy individuals and patients with a pouch without inflammation. As shown by several studies, faecal microbiota transplantation (FMT) with administration of faeces from healthy donors can alter the microbiota. Treatment with faecal microbiota transplantation to chronic pouchitis has been investigated in several clinical trials with mixed results. It is however still uncertain if faecal microbiota transplantation using stool from healthy individuals with a colon is optimal, or if stool from patient with a normally functioning pouch should be used. The study primary aims to investigate if transplantation of faeces from patient with a normal pouch function can induce clinical remission in patients with chronic pouchitis.
Detailed Description
Hypothesis: Gut dysbiosis plays a significant causal role in chronic pouchitis. Modulating the gut microbiota using FMT with stool from a normal function pouch patient has a clinical effect by inducing clinical remission in patients with chronic pouchitis. Objective of the study: The aim of the trial is to investigate if transplantation (FMT) of faeces from a patient with a normally functioning pouch can induce clinical remission in patients with chronic pouchitis. Study design: The project is designed as a single-center, open-label, treatment study. Methods: Faecal microbiota transplantation is performed with faeces from a donor with a normally functioning pouch. Potential donors are recruited from the Department of Gastrointestinal Surgery, Aalborg University Hospital, Denmark. They are screened for a various of infectious diseases by serum analysis (haematology, inflammation, liver and kidney function, HIV, Hepatitis, Cytomegalovirus, Epstein Barr virus and HbA1c) and faeces analysis (calprotectin, Clostridium difficile (PCR), enteric pathogenic bacteria and antibiotic-resistant bacteria, parasites, cysts, and viruses). Furthermore, the potential donors will complete an extensive questionnaire regarding general health, risk factors and medical history, before they can be included as faecal donors in the project. The screening procedure is based on recommendation from the European FMT Working Group. The transplantation is performed by enemas, which contain faeces from the faecal donor. Initial before the treatment with FMT, the patient will be invited for serum analysis (CRP, leukocytes) and faecal analysis (calprotectin, C.difficile, enteric pathogenic bacteria), followed by a pouchoscopy with collection of biopsies. Materials from serum- and faecal analysis and biopsies will be stored for later analysis purpose. The patient will further complete questionnaires concerning symptoms and quality of life. The stage of disease will be evaluated based on the acknowledged questionnaire for pouchitis called Pouchitis Disease Activity Index (PDAI) score. The treatment begins after all the initial examinations, and the patient will be treated during one month. The treatment consists of daily enema infusion, which contain faeces from the faecal donor. During the treatment, the patient will daily record symptoms related to pouchitis (diarrhea, abdominal pain, bleeding per rectum, fever, general discomfort) and possible adverse effects to the treatment. At the end of treatment, the patient will meet to a follow-up examination including serum analysis (CRP, leukocytes) and faecal analysis (calprotectin), pouchoscopy incl. biopsies, and the questionnaires applied before the treatment. Materials from serum- and faecal analysis and biopsies will be stored for later analysis. The patient will be followed up after additional 1,3, 6 and 12 months to evaluate the long term effect of the transplantation. The consumption of antibiotics during the first year will be recorded. In case of lacking effect of faecal microbiota transplantation, the patient is offered standard antibiotic treatment for pouchitis, and will leave the study. Faecal samples and biopsies collected in the study will be analyzed for the composition of the microbiota.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pouchitis, Inflammatory Bowel Diseases, Ulcerative Colitis
Keywords
FMT, Microbiota

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
3 (Actual)

8. Arms, Groups, and Interventions

Arm Title
FMT
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
Faecal microbiota transplantation
Intervention Description
FMT by daily enema with donor faeces
Primary Outcome Measure Information:
Title
Number of patients achieving clinical remission assessed by PDAI
Description
Clinical remission is defined as PDAI<7
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Number of patients achieving clinical response assessed by PDAI
Description
Clinical response is defined as reduction of PDAI score >2
Time Frame
4 weeks
Title
Engraftment of the donor microbiota in the patients
Description
Assessed by beta-diversity
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients ≥ 18 years of age with a J-pouch PDAI ≥ 7 Established diagnosis of chronic pouchitis (≥3 times of pouchitis within the last year, symptoms more than 4 weeks despite antibiotic treatment) Antibiotic treatment for pouchitis (ciprofloxacin and/or metronidazole) within the 3 months Exclusion Criteria: Immunosuppression Pregnancy or breastfeeding Evidence of intestinal pathogen bacteria in the stool at inclusion visit Any severe or newly diagnosed concomitant cardiovascular, hepatic, intestinal, renal, endocrine, pulmonary, dental disease with inflammation or psychiatric disorder, which, in the opinion of the investigator, might have an influence on the patient's compliance or the interpretation of the results Probiotic intake within the last 2 weeks prior to study intervention Participation in another clinical trial within the previous 30 days before baseline Serious food allergies with earlier anaphylactic reactions
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ole Thorlacius-Ussing, Professor
Organizational Affiliation
Aalborg University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Gastrointestinal Surgery, Aalborg University Hospital
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Faecal Microbiota Transplantation From Normal Pouch Function Donor in the Treatment of Chronic Pouchitis

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