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Fecal Microbiota Transplantation for Chronic Pouchitis

Primary Purpose

Ulcerative Colitis, Pouchitis

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Donor FMT
Sponsored by
Aalborg University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis focused on measuring Ulcerative Colitis, Inflammatory bowel disease, Pouchitis, Fecal microbiota transplant, Fecal microbiota treatment

Eligibility Criteria

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

Inclusion Criteria:

  • minimum 18 years old, pouch > 1 year
  • at least three pouchitis events in the past year
  • antibiotic treatment for pouchitis at least one time in the past year

Exclusion Criteria:

  • immunosuppression, pregnancy, detection of specific pathogens in stool

Sites / Locations

  • Research Unit, Department of Gastrointestinal Surgery

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Donor FMT

Arm Description

Fecal transplant from unrelated, healthy volunteers

Outcomes

Primary Outcome Measures

Cure 30 days following FMT treatment
PDAI < 7

Secondary Outcome Measures

Changes of the microbiota
Changes in diversity of gut microbiota after FMT assessed by Shannon index
Clinical response 30 days after FMT treatment
Decrease from baseline PDAI > 2 points
Histological remission following PDAI
Remission of microscopic inflammation
Improvement of pouch function
Improvement of the self-reported questionnaire
Improvement of quality of life
Improvement of the self-reported questionnaire
Improvement of sexuality
Improvement of the self-reported questionnaire

Full Information

First Posted
May 11, 2018
Last Updated
December 17, 2019
Sponsor
Aalborg University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03538366
Brief Title
Fecal Microbiota Transplantation for Chronic Pouchitis
Official Title
Fecal Microbiota Transplantation for the Treatment of Chronic Pouchitis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2019
Overall Recruitment Status
Completed
Study Start Date
May 15, 2018 (Actual)
Primary Completion Date
May 1, 2019 (Actual)
Study Completion Date
May 1, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Aalborg University Hospital

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
Patients with chronic pouchitis are treated with fecal transplant from several unrelated, healthy donors. The treatment consists of enemas of 100 mL fecal suspension, applied for 14 consecutive days.
Detailed Description
Background: The surgical treatment of choice for the treatment of medically refractory ulcerative colitis (UC) is restorative ileal pouch-anal anastomosis (IPAA), in which the patient retains fecal continence following colonectomy, by subsequent anastomosis of the terminal ileum and the rectum. Up to 25% of patients with UC will undergo IPAA surgery. The most common complication following the procedure is inflammation of the pouch (pouchitis), which is seen in up to 50% of patients within the first five years of surgery. Of these patients, 10-20% will develop a chronic inflammatory condition. The clinical symptoms of pouchitis include diarrhea, rectal bleeding, stomach cramps, general malaise and reduced quality of life. Endoscopic findings include mucosal edema, granulations, and ulcerations with mucosal frailty. In most cases, a causative microorganism is not identified, although infection with Clostridium difficile or Cytomegalovirus (CMV) have been reported. The most common treatment of pouchitis is empiric antibiotics, usually quinolones and metronidazole, or a combination of both. Following complications, removal of the pouch can become a last resort, and chronic pouchitis is the leading indication for 10% of these operations. The composition of microbes in the gut is known to be a key factor in the homeostasis of the intestine, and plays a central role in the development of CIBD. Different single microorganisms have previously been suggested as playing an important role in this development, including: Mycobacterium avium, Escherichia coli and Clostridium difficile, that all have invasive capabilities. Several studies have investigated the connection between the composition of microbes in the gut and development of pouchitis finding an increasing evidence for a link between dysbiosis and pouchitis. Method: Patients with chronic pouchitis are treated with fecal transplants from unrelated, healthy donors. The fecal transplant is from several healthy donors. The treatments are applied as enemas of 100 ml suspension for 14 consecutive days. Prior to treatment, pouchitis activity is graded using the pouchitis disease activity index (PDAI) based on symptoms, endoscopic and histological criteria. Patients will also complete self-reported questionnaires regarding pouch function, quality of life and sexuality. Patients are evaluated using the PDAI score 30 days following treatment together with the self-reported questionnaires. Longterm follow up is evaluated up to 6 months following FMT. Screening of FMT donors: Questionaire regarding possible contagious infectious diseases, followed by interview with principal investigator. Blood test for: inflammatory parameters: CRP, leucocyte count, HIV 1+2 antigen, Hepatitis A, B and C, CMV, EBV and HbA1c Fecal samples: Calprotectin Pathogenic bacteria (Salmonella, Campylobacter, Yersinia, Shigella), Vibrio, toxin-producing E. coli. Parasites, giardia spp. and cryptosporidium spp. Adenovirus, enterovirus, parechovirus Clostridium difficile Vancomycin-resistent Enterococcus faecalis and Enterococcus faecium, carbapenemase-producing enterobacteria and ESBL-producing E.coli. FMT donor exclusion criteria are: Age <20 or >65 BMI <18.5 or > 28.0 kg/m2 Known chronic inflammatory bowel disease, celiac disease, rheumatoid arthritis or other autoimmune disease, sclerosis, psoriasis, previous extensive bowel surgery In the previous 6 months: Diarrhea > 3 days in one week or bloody stools Treatment with antibiotics Risk of sexually transmitted disease, tattoos, piercings, travel to areas with high endemic transmission of infectious diseases or resistants microbes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis, Pouchitis
Keywords
Ulcerative Colitis, Inflammatory bowel disease, Pouchitis, Fecal microbiota transplant, Fecal microbiota treatment

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Donor FMT
Arm Type
Experimental
Arm Description
Fecal transplant from unrelated, healthy volunteers
Intervention Type
Other
Intervention Name(s)
Donor FMT
Intervention Description
Fecal transplant from unrelated, healthy donors using enemas
Primary Outcome Measure Information:
Title
Cure 30 days following FMT treatment
Description
PDAI < 7
Time Frame
30 days
Secondary Outcome Measure Information:
Title
Changes of the microbiota
Description
Changes in diversity of gut microbiota after FMT assessed by Shannon index
Time Frame
30 days
Title
Clinical response 30 days after FMT treatment
Description
Decrease from baseline PDAI > 2 points
Time Frame
30 days
Title
Histological remission following PDAI
Description
Remission of microscopic inflammation
Time Frame
30 days
Title
Improvement of pouch function
Description
Improvement of the self-reported questionnaire
Time Frame
30 days
Title
Improvement of quality of life
Description
Improvement of the self-reported questionnaire
Time Frame
30 days
Title
Improvement of sexuality
Description
Improvement of the self-reported questionnaire
Time Frame
30 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: minimum 18 years old, pouch > 1 year at least three pouchitis events in the past year antibiotic treatment for pouchitis at least one time in the past year Exclusion Criteria: immunosuppression, pregnancy, detection of specific pathogens in stool
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ole Thorlacius-Ussing, Professor
Organizational Affiliation
Aalborg University Hospital, Aalborg University
Official's Role
Study Director
Facility Information:
Facility Name
Research Unit, Department of Gastrointestinal Surgery
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
10372273
Citation
Becker JM. Surgical therapy for ulcerative colitis and Crohn's disease. Gastroenterol Clin North Am. 1999 Jun;28(2):371-90, viii-ix. doi: 10.1016/s0889-8553(05)70061-3.
Results Reference
background
PubMed Identifier
14703744
Citation
Onaitis MW, Mantyh C. Ileal pouch-anal anastomosis for ulcerative colitis and familial adenomatous polyposis: historical development and current status. Ann Surg. 2003 Dec;238(6 Suppl):S42-8. doi: 10.1097/01.sla.0000098115.90865.16.
Results Reference
background
PubMed Identifier
16830218
Citation
Lovegrove RE, Tilney HS, Heriot AG, von Roon AC, Athanasiou T, Church J, Fazio VW, Tekkis PP. A comparison of adverse events and functional outcomes after restorative proctocolectomy for familial adenomatous polyposis and ulcerative colitis. Dis Colon Rectum. 2006 Sep;49(9):1293-306. doi: 10.1007/s10350-006-0608-0.
Results Reference
background
PubMed Identifier
7958702
Citation
Sandborn WJ. Pouchitis following ileal pouch-anal anastomosis: definition, pathogenesis, and treatment. Gastroenterology. 1994 Dec;107(6):1856-60. doi: 10.1016/0016-5085(94)90832-x. No abstract available.
Results Reference
background
PubMed Identifier
12600225
Citation
Shen B. Diagnosis and treatment of patients with pouchitis. Drugs. 2003;63(5):453-61. doi: 10.2165/00003495-200363050-00002.
Results Reference
background
PubMed Identifier
11720319
Citation
Shen B, Achkar JP, Lashner BA, Ormsby AH, Remzi FH, Brzezinski A, Bevins CL, Bambrick ML, Seidner DL, Fazio VW. A randomized clinical trial of ciprofloxacin and metronidazole to treat acute pouchitis. Inflamm Bowel Dis. 2001 Nov;7(4):301-5. doi: 10.1097/00054725-200111000-00004.
Results Reference
background
PubMed Identifier
15578518
Citation
Sandborn WJ, Pardi DS. Clinical management of pouchitis. Gastroenterology. 2004 Dec;127(6):1809-14. doi: 10.1053/j.gastro.2004.10.011. No abstract available.
Results Reference
background
PubMed Identifier
21407187
Citation
Khan KJ, Ullman TA, Ford AC, Abreu MT, Abadir A, Marshall JK, Talley NJ, Moayyedi P. Antibiotic therapy in inflammatory bowel disease: a systematic review and meta-analysis. Am J Gastroenterol. 2011 Apr;106(4):661-73. doi: 10.1038/ajg.2011.72. Epub 2011 Mar 15. Erratum In: Am J Gastroenterol. 2011 May;106(5):1014. Abadir, A [corrected to Abadir, Amir].
Results Reference
background
PubMed Identifier
12894016
Citation
Tulchinsky H, Hawley PR, Nicholls J. Long-term failure after restorative proctocolectomy for ulcerative colitis. Ann Surg. 2003 Aug;238(2):229-34. doi: 10.1097/01.sla.0000082121.84763.4c.
Results Reference
background
PubMed Identifier
25110406
Citation
Angriman I, Scarpa M, Castagliuolo I. Relationship between pouch microbiota and pouchitis following restorative proctocolectomy for ulcerative colitis. World J Gastroenterol. 2014 Aug 7;20(29):9665-74. doi: 10.3748/wjg.v20.i29.9665.
Results Reference
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Fecal Microbiota Transplantation for Chronic Pouchitis

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