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Fecal Transplantation Using a Diet for Donor and Recipient in Refractory Colitis

Primary Purpose

Ulcerative Colitis

Status
Terminated
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Fecal transplantation
Unique novel Diet for UC and Unique novel Diet for the donor + FMT
Unique novel Diet for UC
Sponsored by
Wolfson Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ulcerative Colitis focused on measuring Ulcerative Colitis, Nutrition, microbiome

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Informed consent
  2. Established diagnosis of UC, disease confined to the large intestine, involving the rectosigmoid for at least 3 months.
  3. Age: 18 - 70 years ( inclusive)
  4. Mild to Moderate active disease, SCCAI of ≥5 and <10 with endoscopic subscore≥2
  5. Refractory to mesalamine 6 weeks, or steroids > 14 days, or immunomodulator 12 weeks or biologics at least 12 weeks therapy.
  6. No use or stable use for 2 weeks of medical cannabis.

Inclusion criteria Comments:

1. Patients can enter the trial if they are on steroids if they have been treated for at least two weeks with 40 mg prednisone or an intravenous steroid such as methylprednisolone and still suffer from a mild to moderate active disease.

Exclusion Criteria:

  1. Start of a new biologic in the previous 12 weeks.
  2. Evidence for Clostridium difficile infection.
  3. Any proven current infection such as CMV, positive stool culture or parasite.
  4. Current Extra intestinal manifestation of UC such as active arthritis or primary sclerosing cholangitis (PSC).
  5. Immune deficiency (other than drug induced).
  6. Current use of a calcineurin inhibitor
  7. Pregnancy.
  8. Suspected toxic megacolon, guarding on palpation, or signs of peritoneal inflammation
  9. Patients with other IBD unrelated disease such as autoimmune disorders, renal failure, fever or current infection (UTI, strep throat, pneumonia, etc), prior or current neoplasia
  10. Fecal Transplantation in the last 6 months.
  11. Fever >38
  12. Participation in another clinical interventional trial
  13. An active malignant disease or a prior malignancy during the previous 5 years (excluding skin BCC).
  14. Inability or reluctance to use an enema.
  15. Anticipation for antibiotic use within the study period (such as for elective surgery or dental treatment).
  16. Acute severe UC in the past 3 months.
  17. Presence of a pouch or pouchitis.
  18. Patients > 60 years old using chronic medications except for the treatment for colitis.

Exclusion criteria Comments:

  • Patients will be excluded from the analysis if during the study and after the initial fecal transplant they did not perform the enemas, used antibiotics prior to day 42. Patients who required additional therapy such as additional FMT, steroids biologics or immunomodulators during the first 8 weeks will be considered failures on an intention to treat basis.
  • Patients with mayo< 2 at the baseline colonoscopy may receive the FMT and continue the follow up according to the protocol as an open lable based on the randomization. Those patients will be excluded from the final analysis.

Special populations (e.g children, unable to sign an informed consent, those under a guardian) and pregnant women will also be excluded.

Donors:

Donors will sign an informed consent and will be screened and included only if they satisfy the rigorous screening criteria of the protocol of the Ministry of Health of Israel for stool donors for Clostridium difficile infection which includes a list of medical and behavioral conditions as well as transmissible pathogens that need to be screened by history, anthropometry, blood and stool tests (available as supplement).

Sites / Locations

  • Saint-Antoine Hospital, Universite Pierre et Marie Curie
  • Wolfson Medical Center
  • Tel Aviv Sourasky Medical Center
  • Humanitas Clinical and Research Center
  • Catholic University of the Secret Heart

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Active Comparator

Arm Label

Fecal microbiota transplantation (FMT) without Diet

FMT with Diet for the donor and for the recipient

Dietary therapy only

Arm Description

undergo standard fecal transplantation by colonoscopy on day 1 and 60 ml rectal enemas on days 2 and 14 from the same donor without dietary conditioning.

undergo standard fecal transplantation by colonoscopy on day 1 and 60 ml rectal enemas on days 2 and 14 with dietary pre-conditioning of the donor for 14 days and dietary treatment of the recipient immediately after transplantation and for the following 12 weeks.

The patient will receive detailed instructions regarding the UC diet to be used over 12 weeks without FMT.

Outcomes

Primary Outcome Measures

Clinical remission
determined by Simple Clinical Colitis Activity Index (SCCAI) score <3 at week 8

Secondary Outcome Measures

Improvement
Improvement in the Simple Clinical Colitis Activity Index (SCCAI) score at weeks 8 & 12 for each of the groups
Endoscopic resutls
Mayo endoscopic score <2 (for patients performing sigmoidoscopy)
Calprotectin
Calprotectin < 250 µg/g
The need for additional therapy or flare
According to the physician discretion
change in the microbiome compared to baseline.
According to analysis of fecal samples
endoscopic SCCAI
endoscopic SCCAI score at week 8 for each of the groups

Full Information

First Posted
March 28, 2016
Last Updated
May 29, 2022
Sponsor
Wolfson Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02734589
Brief Title
Fecal Transplantation Using a Diet for Donor and Recipient in Refractory Colitis
Official Title
Fecal Transplantation Using a Novel Conditioning Method for Donor and Recipient in Mild to Moderate Treatment Refractory Colitis in Inflammatory Bowel Disease
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Terminated
Why Stopped
DSMB recommendation of stopping the trial after reviewing the interim data
Study Start Date
January 24, 2017 (Actual)
Primary Completion Date
December 30, 2020 (Actual)
Study Completion Date
December 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wolfson Medical Center

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
Changing the microbiota has become the most intriguing target for intervention in inflammatory bowel disease (IBD). Dietary therapy is successful in mild to moderate Crohn's disease and may be effective in mild to moderate ulcerative colitis (UC) as well, though dietary interventions in UC are just getting underway. However these interventions are less likely to be effective for the more severely inflamed or refractory end of the spectrum. Fecal transplantation (FT) has been suggested as a method to treat refractory IBD, but most studies have been unsuccessful in establishing remission and especially sustained remission. The investigators hypothesize that this is due to selection of random donors and the inability to maintain an optimal microbiota eco system post transplant. Diet is a powerful tool to modulate the microbiota. The investigators propose that use of a donor and recipient diet designed for UC during fecal transplantation will be superior to diet alone of fecal transplantation alone and will improve patient outcomes.The investigators propose to modify FT using a novel protocol and approach that we have developed. We have developed a unique diet that is geared to rectify dysbiosis in UC and damage to the mucous layer in active UC. The investigators intend to condition both donor and recipient with the diet to achieve optimal conditions for transplant to succeed for both donor and recipient .The investigators intend to evaluate this protocol in adults with active UC that are refractory to medications. The investigators will start with a randomized controlled trial involving 76 transplanted patients+ 20 subjects for dietary controls with the UC diet alone.
Detailed Description
Study type- It will be an open label 3 arm multicenter randomized controlled single blinded study, with review of endoscopic activity by blinded reviewers. Patients will be randomized to one of three groups; Group 1 will undergo standard fecal transplantation by colonoscopy on day 1 and 60 ml rectal enemas on days 2 and 14 from the same donor without dietary conditioning, while Group 2 will undergo the same transplantation (colonoscopy and enemas at night day 2 and day 14), with dietary pre-conditioning of the donor for 14 days and dietary treatment of the recipient immediately after transplantation and for the following 12 weeks.We will attempt to use the same donors for group 1 and 2 by using the preconditioning stool for group 1 and the post conditioning stool for group 2 in order to control for the "donor effect". Group 3 will receive dietary therapy only.Physicians will be blinded to treatment arm and donors used within the transplantation arms. A data safety monitoring board will review safety after the first 34 patients to make sure that there is no ethical problem with continuing the study. The investigators will continue the fecal transplantation trial to reach our target enrolment number ( 76 patients) for transplantation + 20 dietary controls. Subjects may continue their stable medications but should not start new medications during the 8 week period unless they fail to respond. Steroid weaning can commenced from day 14. Patients will be seen on weeks0, 2, 6, 8, 12 and during week 20. Week 6 will be only a dietitian visit. The last visit is a visit off diet to evaluate sustainability of the initial intervention, safety and changes in BMI due to FT or diet. A telephone conversation to assess SCCAI will be made at week 1 and week 7. At each visit (weeks 0, 2, 6, 8, 12, 20) patients will have Weight, a disease activity score, PGA, CBC, CRP, albumin and complete chemistry panel performed. Adverse events and medications used will be recorded at each visit.Stool samples for microbiome (16S rDNA, Short chain fatty acid analysis) and Calprotectin will be measured locally at baseline, weeks 2, 8 and 12. All patients (patients in group 1,2 and 3) will have a repeat sigmoidoscopy performed at week 8. A food frequency questionnaire will be performed on week 0 and a food diary will be collected at week 2 and 12. A compliance questionnaire will be completed on weeks 2, 8and 12. A 24 hours recall will be collected at weeks 0, 2 and 6. Patients in group 1 or 2 in remission from FT, may receive up to 2 rescue enemas during the 8 weeks of the study from their original donor.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
Keywords
Ulcerative Colitis, Nutrition, microbiome

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Masking Description
single blind
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Fecal microbiota transplantation (FMT) without Diet
Arm Type
Active Comparator
Arm Description
undergo standard fecal transplantation by colonoscopy on day 1 and 60 ml rectal enemas on days 2 and 14 from the same donor without dietary conditioning.
Arm Title
FMT with Diet for the donor and for the recipient
Arm Type
Experimental
Arm Description
undergo standard fecal transplantation by colonoscopy on day 1 and 60 ml rectal enemas on days 2 and 14 with dietary pre-conditioning of the donor for 14 days and dietary treatment of the recipient immediately after transplantation and for the following 12 weeks.
Arm Title
Dietary therapy only
Arm Type
Active Comparator
Arm Description
The patient will receive detailed instructions regarding the UC diet to be used over 12 weeks without FMT.
Intervention Type
Other
Intervention Name(s)
Fecal transplantation
Other Intervention Name(s)
Fecal microbiota transplantation (FMT)
Intervention Description
Transplantation of fecal bacteria from a healthy individual into a recipient- ulcerative colitis patient via colonoscopy and enemas
Intervention Type
Other
Intervention Name(s)
Unique novel Diet for UC and Unique novel Diet for the donor + FMT
Other Intervention Name(s)
Ulcerative Colitis Diet (UCD) and the conditioning diet
Intervention Description
A developed unique diet that is geared to induces remission and decreases inflammation in patients with active UC. Also a conditioning diet for healthy subjects to be used by the donor prior to transplantation- a developed unique diet for two weeks.
Intervention Type
Other
Intervention Name(s)
Unique novel Diet for UC
Other Intervention Name(s)
Ulcerative Colitis Diet (UCD)
Intervention Description
A developed diet that is geared to induces remission and decreases inflammation in patients with active UC.
Primary Outcome Measure Information:
Title
Clinical remission
Description
determined by Simple Clinical Colitis Activity Index (SCCAI) score <3 at week 8
Time Frame
Day 56
Secondary Outcome Measure Information:
Title
Improvement
Description
Improvement in the Simple Clinical Colitis Activity Index (SCCAI) score at weeks 8 & 12 for each of the groups
Time Frame
Days 56 & 84
Title
Endoscopic resutls
Description
Mayo endoscopic score <2 (for patients performing sigmoidoscopy)
Time Frame
Day 56
Title
Calprotectin
Description
Calprotectin < 250 µg/g
Time Frame
Day 56
Title
The need for additional therapy or flare
Description
According to the physician discretion
Time Frame
Week 12
Title
change in the microbiome compared to baseline.
Description
According to analysis of fecal samples
Time Frame
For donor- day 14 and for recipient day 56
Title
endoscopic SCCAI
Description
endoscopic SCCAI score at week 8 for each of the groups
Time Frame
Day 56

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent Established diagnosis of UC, disease confined to the large intestine, involving the rectosigmoid for at least 3 months. Age: 18 - 70 years ( inclusive) Mild to Moderate active disease, SCCAI of ≥5 and <10 with endoscopic subscore≥2 Refractory to mesalamine 6 weeks, or steroids > 14 days, or immunomodulator 12 weeks or biologics at least 12 weeks therapy. No use or stable use for 2 weeks of medical cannabis. Inclusion criteria Comments: 1. Patients can enter the trial if they are on steroids if they have been treated for at least two weeks with 40 mg prednisone or an intravenous steroid such as methylprednisolone and still suffer from a mild to moderate active disease. Exclusion Criteria: Start of a new biologic in the previous 12 weeks. Evidence for Clostridium difficile infection. Any proven current infection such as CMV, positive stool culture or parasite. Current Extra intestinal manifestation of UC such as active arthritis or primary sclerosing cholangitis (PSC). Immune deficiency (other than drug induced). Current use of a calcineurin inhibitor Pregnancy. Suspected toxic megacolon, guarding on palpation, or signs of peritoneal inflammation Patients with other IBD unrelated disease such as autoimmune disorders, renal failure, fever or current infection (UTI, strep throat, pneumonia, etc), prior or current neoplasia Fecal Transplantation in the last 6 months. Fever >38 Participation in another clinical interventional trial An active malignant disease or a prior malignancy during the previous 5 years (excluding skin BCC). Inability or reluctance to use an enema. Anticipation for antibiotic use within the study period (such as for elective surgery or dental treatment). Acute severe UC in the past 3 months. Presence of a pouch or pouchitis. Patients > 60 years old using chronic medications except for the treatment for colitis. Exclusion criteria Comments: Patients will be excluded from the analysis if during the study and after the initial fecal transplant they did not perform the enemas, used antibiotics prior to day 42. Patients who required additional therapy such as additional FMT, steroids biologics or immunomodulators during the first 8 weeks will be considered failures on an intention to treat basis. Patients with mayo< 2 at the baseline colonoscopy may receive the FMT and continue the follow up according to the protocol as an open lable based on the randomization. Those patients will be excluded from the final analysis. Special populations (e.g children, unable to sign an informed consent, those under a guardian) and pregnant women will also be excluded. Donors: Donors will sign an informed consent and will be screened and included only if they satisfy the rigorous screening criteria of the protocol of the Ministry of Health of Israel for stool donors for Clostridium difficile infection which includes a list of medical and behavioral conditions as well as transmissible pathogens that need to be screened by history, anthropometry, blood and stool tests (available as supplement).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arie Levine, MD
Organizational Affiliation
Wolfson Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Yona Avni, MD
Organizational Affiliation
Wolfson Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Saint-Antoine Hospital, Universite Pierre et Marie Curie
City
Paris
ZIP/Postal Code
75571
Country
France
Facility Name
Wolfson Medical Center
City
Holon
ZIP/Postal Code
58100
Country
Israel
Facility Name
Tel Aviv Sourasky Medical Center
City
Tel Aviv
Country
Israel
Facility Name
Humanitas Clinical and Research Center
City
Milan
Country
Italy
Facility Name
Catholic University of the Secret Heart
City
Rome
Country
Italy

12. IPD Sharing Statement

Citations:
PubMed Identifier
34514495
Citation
Sarbagili Shabat C, Scaldaferri F, Zittan E, Hirsch A, Mentella MC, Musca T, Cohen NA, Ron Y, Fliss Isakov N, Pfeffer J, Yaakov M, Fanali C, Turchini L, Masucci L, Quaranta G, Kolonimos N, Godneva A, Weinberger A, Kopylov U, Levine A, Maharshak N. Use of Faecal Transplantation with a Novel Diet for Mild to Moderate Active Ulcerative Colitis: The CRAFT UC Randomised Controlled Trial. J Crohns Colitis. 2022 Mar 14;16(3):369-378. doi: 10.1093/ecco-jcc/jjab165.
Results Reference
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Fecal Transplantation Using a Diet for Donor and Recipient in Refractory Colitis

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