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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.
Enrollment
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Inclusion and exclusion criteria
Participant Inclusion Criteria:
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
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
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:
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:
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20 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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