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Gut Microbial Transplantation in Pediatric Inflammatory Bowel Diseases (GMT)

Primary Purpose

Inflammatory Bowel Disease (IBD)

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Gut Microbial Transplantation
Sponsored by
Spectrum Health Hospitals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Inflammatory Bowel Disease (IBD) focused on measuring ulcerative colitis, gut microbial transplantation

Eligibility Criteria

7 Years - 21 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Participant Inclusion Criteria:

  1. Children ages >7 and ≤21 years of age with established diagnosis of Inflammatory Bowel Disease (IBD) colitis (patient with ulcerative colitis (UC) or patients with crohn's disease (CD) with colonic involvement only)
  2. Have clinical disease (mild to moderate disease: 10≤ Pediatric Ulcerative Colitis Activity Index (PUCAI) <65)
  3. Have stable disease activity and therapy for two months prior to Gut Microbial Transplantation (GMT) procedure.

Participant Exclusion Criteria:

  1. Fulminant colitis
  2. Indication or scheduled for surgery
  3. Pregnancy
  4. Use of probiotic supplements during the study period (subjects who have stopped use of probiotic supplements will be eligible as long as they stop taking it 2 weeks prior to Day 1 of GMT)
  5. anemia (hemoglobin < 6.0 g/dL) in last one month
  6. Graft versus host disease (GVHD)
  7. Severely immunocompromised - defined as

    1. History of opportunistic infection (tuberculosis, Pneumocystis jirovecii or systemic fungal infections) in last one year or
    2. Neutropenia: Absolute neutrophil count (ANC) <500
  8. Major intra-abdominal surgery within 90 days prior to Day 1 of GMT
  9. Administration of any investigational drug within 30 days prior to Day 1 of GMT.
  10. Have received infliximab or other tumor necrosis factor (TNF) inhibitors within 2 months prior to Day 1 of GMT or are expected to receive such therapy within 1 month post final GMT.

Donor Inclusion Criteria

  1. Based on patient's and parents'/guardian's decision
  2. Will be chosen from immediate adult (≥18 years) family members or close friends
  3. Should have negative or normal results on screening tests (as explained in donor exclusion criteria below)

Donor Exclusion Criteria (adopted from guidelines provided by American Association of Blood Bank Donor History Questionnaire and American Gastroenterological Association)

  1. Positive or abnormal screening test to include:

    1. Hepatitis A Immunoglobulin M (IgM) antibody
    2. Hepatitis B antibody panel suggestive of infection (HBc IgM, HBs Ag, HBs Ab)
    3. Hepatitis C antibody Level
    4. Cytomegalovirus (CMV) IgM antibody
    5. Ebstein Barr Virus (EBV) viral capsid antigen (VCA) IgM antibody
    6. Syphilis Immunoglobulin G (IgG) Ab Screen
    7. Human Immune Deficiency Virus (HIV) I & II enzyme-linked immunosorbent assay (ELISA) screen
    8. Stool i) Fungal smear ii) Stool cultures to exclude Salmonella, Shigella, Escherichia Coli, Campylobacter, Yersinia, Vibrio, Listeria iii) Clostridium difficile toxin assay iv) Ova and parasite screen for Giardia and Cryptosporidium
  2. History of metabolic syndrome or gastric bypass surgery
  3. History of GI conditions: IBD, irritable bowel syndrome, chronic abdominal pain, GI Malignancy, blood in stool or diarrhea in the last 4 weeks before enrollment
  4. Antibiotic or probiotic use within 3 months before enrollment and for the duration of the donation
  5. Positive response on screening questionnaire to any of the following:

    1. History of active malignancy or any cancer within the last 5 years (excluding basal cell carcinoma of the skin)
    2. Family history of Creutzfeld-Jacob disease
    3. Corneal or dural transplant
    4. History of high risk sexual behavior (e.g. sexual contact with HIV/acquired immune deficiency syndrome (AIDS) positive, hepatitis positive partner, men who have sex with men, sex for drugs or money)
    5. History of signs of sexually transmitted infections such as genital ulcerations, anogenital herpes, anogenital warts, cancroids or syphilitic lesions
    6. Use of illicit drugs
    7. Travel within the last 6 months to areas of the world where diarrheal illnesses are endemic
    8. History or signs of immunosuppression i) History of any immunosuppressant medication(s) within the last 6 months or history of opportunistic infection(s) in past 1 year ii) Signs of immunosuppression such as:
    1. Oral thrush
    2. Disseminated lymphadenopathy

Sites / Locations

  • Helen DeVos Children's Hospital of Spectrum Health Hospitals

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Study Participants

Arm Description

Participants did not receive any bowel preparation before Gut Microbial Transplantation (GMT). Audio-visual aids were used to help reduce participants' anxiety about GMT.

Outcomes

Primary Outcome Measures

Clinical Response
Clinical response (i.e. improvement in Pediatric Ulcerative Colitis Activity Index (PUCAI) score by greater than or equal to 15 points from baseline) at 4 weeks following GMT treatment

Secondary Outcome Measures

Full Information

First Posted
March 20, 2012
Last Updated
May 31, 2023
Sponsor
Spectrum Health Hospitals
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1. Study Identification

Unique Protocol Identification Number
NCT01560819
Brief Title
Gut Microbial Transplantation in Pediatric Inflammatory Bowel Diseases
Acronym
GMT
Official Title
Gut Microbial Transplantation in Pediatric Inflammatory Bowel Diseases
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
March 2012 (undefined)
Primary Completion Date
December 2012 (Actual)
Study Completion Date
June 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Spectrum Health Hospitals

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Inflammatory bowel disease (IBD) is a chronic, debilitating, relapsing inflammatory disorder affecting the gastrointestinal tract which does not have a medical cure. IBD consists of 2 different forms: Crohn's Disease (CD) and Ulcerative Colitis (UC). In the last 2 decades, Gut Microbial Transplantation (GMT), also known as fecal transplantation, has been used as a treatment option for Clostridium difficile colitis and UC. The literature supports strong evidence for the plausibility of using GMT for patients with IBD associated colitis, especially for patients with UC. This research will be conducted in the Helen DeVos Children's Hospital (HDVCH) Pediatric gastrointestinal outpatient clinic. A pilot study of ten patients will be conducted to evaluate if GMT improves clinical symptoms in patients with IBD. Patients with IBD colitis (UC and CD with colonic involvement only) will be approached for GMT as a treatment option for their disease. Each subject will undergo 5 sessions (1 session/day, and not necessarily on consecutive days) of GMT within a period of 10 days. Post treatment evaluation will be done at their regularly scheduled clinic follow up. Healthy donors >18 years of age will be chosen by the family, inclusive of immediate family members and friends. Donors will be required to complete a screening questionnaire, provide medical history, and undergo blood and stool tests.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Inflammatory Bowel Disease (IBD)
Keywords
ulcerative colitis, gut microbial transplantation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Study Participants
Arm Type
Experimental
Arm Description
Participants did not receive any bowel preparation before Gut Microbial Transplantation (GMT). Audio-visual aids were used to help reduce participants' anxiety about GMT.
Intervention Type
Drug
Intervention Name(s)
Gut Microbial Transplantation
Other Intervention Name(s)
GMT
Intervention Description
Each participant received Gut Microbial Transplantation (GMT) as retention enema over a period of 1 hour (60mL enema every 15 minutes) daily for 5 days. Although 240mL of GMT solution was prepared for each participant, the final administered dose was dependent on the subject's comfort and willingness to proceed with the next enema, which was assessed after each enema infusion. Subjects were monitored for 30 minutes after GMT for any immediate adverse events and discharged.
Primary Outcome Measure Information:
Title
Clinical Response
Description
Clinical response (i.e. improvement in Pediatric Ulcerative Colitis Activity Index (PUCAI) score by greater than or equal to 15 points from baseline) at 4 weeks following GMT treatment
Time Frame
4 weeks following GMT Treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
7 Years
Maximum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Participant Inclusion Criteria: Children ages >7 and ≤21 years of age with established diagnosis of Inflammatory Bowel Disease (IBD) colitis (patient with ulcerative colitis (UC) or patients with crohn's disease (CD) with colonic involvement only) Have clinical disease (mild to moderate disease: 10≤ Pediatric Ulcerative Colitis Activity Index (PUCAI) <65) Have stable disease activity and therapy for two months prior to Gut Microbial Transplantation (GMT) procedure. Participant Exclusion Criteria: Fulminant colitis Indication or scheduled for surgery Pregnancy Use of probiotic supplements during the study period (subjects who have stopped use of probiotic supplements will be eligible as long as they stop taking it 2 weeks prior to Day 1 of GMT) anemia (hemoglobin < 6.0 g/dL) in last one month Graft versus host disease (GVHD) Severely immunocompromised - defined as History of opportunistic infection (tuberculosis, Pneumocystis jirovecii or systemic fungal infections) in last one year or Neutropenia: Absolute neutrophil count (ANC) <500 Major intra-abdominal surgery within 90 days prior to Day 1 of GMT Administration of any investigational drug within 30 days prior to Day 1 of GMT. Have received infliximab or other tumor necrosis factor (TNF) inhibitors within 2 months prior to Day 1 of GMT or are expected to receive such therapy within 1 month post final GMT. Donor Inclusion Criteria Based on patient's and parents'/guardian's decision Will be chosen from immediate adult (≥18 years) family members or close friends Should have negative or normal results on screening tests (as explained in donor exclusion criteria below) Donor Exclusion Criteria (adopted from guidelines provided by American Association of Blood Bank Donor History Questionnaire and American Gastroenterological Association) Positive or abnormal screening test to include: Hepatitis A Immunoglobulin M (IgM) antibody Hepatitis B antibody panel suggestive of infection (HBc IgM, HBs Ag, HBs Ab) Hepatitis C antibody Level Cytomegalovirus (CMV) IgM antibody Ebstein Barr Virus (EBV) viral capsid antigen (VCA) IgM antibody Syphilis Immunoglobulin G (IgG) Ab Screen Human Immune Deficiency Virus (HIV) I & II enzyme-linked immunosorbent assay (ELISA) screen Stool i) Fungal smear ii) Stool cultures to exclude Salmonella, Shigella, Escherichia Coli, Campylobacter, Yersinia, Vibrio, Listeria iii) Clostridium difficile toxin assay iv) Ova and parasite screen for Giardia and Cryptosporidium History of metabolic syndrome or gastric bypass surgery History of GI conditions: IBD, irritable bowel syndrome, chronic abdominal pain, GI Malignancy, blood in stool or diarrhea in the last 4 weeks before enrollment Antibiotic or probiotic use within 3 months before enrollment and for the duration of the donation Positive response on screening questionnaire to any of the following: History of active malignancy or any cancer within the last 5 years (excluding basal cell carcinoma of the skin) Family history of Creutzfeld-Jacob disease Corneal or dural transplant History of high risk sexual behavior (e.g. sexual contact with HIV/acquired immune deficiency syndrome (AIDS) positive, hepatitis positive partner, men who have sex with men, sex for drugs or money) History of signs of sexually transmitted infections such as genital ulcerations, anogenital herpes, anogenital warts, cancroids or syphilitic lesions Use of illicit drugs Travel within the last 6 months to areas of the world where diarrheal illnesses are endemic History or signs of immunosuppression i) History of any immunosuppressant medication(s) within the last 6 months or history of opportunistic infection(s) in past 1 year ii) Signs of immunosuppression such as: Oral thrush Disseminated lymphadenopathy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sachin Kunde, MD, MPH
Organizational Affiliation
Helen DeVos Children's Hospital of Spectrum Health Hospitals
Official's Role
Principal Investigator
Facility Information:
Facility Name
Helen DeVos Children's Hospital of Spectrum Health Hospitals
City
Grand Rapids
State/Province
Michigan
ZIP/Postal Code
49503
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23542823
Citation
Kunde S, Pham A, Bonczyk S, Crumb T, Duba M, Conrad H Jr, Cloney D, Kugathasan S. Safety, tolerability, and clinical response after fecal transplantation in children and young adults with ulcerative colitis. J Pediatr Gastroenterol Nutr. 2013 Jun;56(6):597-601. doi: 10.1097/MPG.0b013e318292fa0d.
Results Reference
result

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Gut Microbial Transplantation in Pediatric Inflammatory Bowel Diseases

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