Fecal Microbiota Transplantation in Pediatric Patients
Status: | Active, not recruiting |
---|---|
Conditions: | Colitis, Colitis, Irritable Bowel Syndrome (IBS), Gastrointestinal, Gastrointestinal, Crohns Disease |
Therapuetic Areas: | Gastroenterology |
Healthy: | No |
Age Range: | 2 - 22 |
Updated: | 4/21/2016 |
Start Date: | September 2014 |
End Date: | October 2017 |
A Study of Fecal Microbiota Transplantation in Pediatric Patients With Relapsed Inflammatory Bowel Disease.
A disturbance in the diversity of gut bacterial composition could be linked to several
immune mediated diseases including inflammatory bowel diseases (IBD). IBD can be classified
into Crohn's Disease (CD) and Ulcerative Colitis (UC). Both these diseases occur from
abnormal immune reaction to resident gut bacteria.The process of fecal microbiota
transplantation (FMT) where fecal bacteria from a healthy individual is transferred into a
recipient, has recently received attention as an alternative therapy for individuals
affected with these life-altering diseases. In this study, the investigators will perform
fecal transplantation on the subjects meeting inclusion criteria, to determine the efficacy
and safety of this therapy in subjects with IBD (CD and UC) who are not responding to first
line therapy, and are in a flare.
immune mediated diseases including inflammatory bowel diseases (IBD). IBD can be classified
into Crohn's Disease (CD) and Ulcerative Colitis (UC). Both these diseases occur from
abnormal immune reaction to resident gut bacteria.The process of fecal microbiota
transplantation (FMT) where fecal bacteria from a healthy individual is transferred into a
recipient, has recently received attention as an alternative therapy for individuals
affected with these life-altering diseases. In this study, the investigators will perform
fecal transplantation on the subjects meeting inclusion criteria, to determine the efficacy
and safety of this therapy in subjects with IBD (CD and UC) who are not responding to first
line therapy, and are in a flare.
50 subjects (25 subjects with Crohn's Disease and 25 subjects with Ulcerative Colitis) who
are 2 to 22 years of age will be enrolled in the trial over 3 years. The fecal donors,
preferably a parent or sibling, will be extensively screened for infectious diseases prior
to providing stool for the transplant. Patients who are failing primary therapy, are in a
flare, and require restaging of their IBD by an endoscopy and colonoscopy will be approached
for the study. Standard of care endoscopy and colonoscopy will be performed on each subject
and 2 additional biopsies will be taken for analysis. Microbiota analysis will also be
performed on both the donor and recipient stool sample prior to transplantation, and on the
recipient sample at 1 week, 1 month, and 6 months post transplantation. The primary
objective will be to study the safety of FMT in all enrolled subjects. The study will also
correlate efficacy and patient outcomes with the fecal microbiome prior to, and after FMT.
The secondary objectives are to examine the efficacy of FMT in the treatment of children
with IBD using the Pediatric Ulcerative Colitis Activity Index (PUCAI) and the Pediatric
Crohn Disease Activity Index (PCDAI) analysis. Correlate the patient outcomes with the fecal
microbiome prior to, and after FMT.
are 2 to 22 years of age will be enrolled in the trial over 3 years. The fecal donors,
preferably a parent or sibling, will be extensively screened for infectious diseases prior
to providing stool for the transplant. Patients who are failing primary therapy, are in a
flare, and require restaging of their IBD by an endoscopy and colonoscopy will be approached
for the study. Standard of care endoscopy and colonoscopy will be performed on each subject
and 2 additional biopsies will be taken for analysis. Microbiota analysis will also be
performed on both the donor and recipient stool sample prior to transplantation, and on the
recipient sample at 1 week, 1 month, and 6 months post transplantation. The primary
objective will be to study the safety of FMT in all enrolled subjects. The study will also
correlate efficacy and patient outcomes with the fecal microbiome prior to, and after FMT.
The secondary objectives are to examine the efficacy of FMT in the treatment of children
with IBD using the Pediatric Ulcerative Colitis Activity Index (PUCAI) and the Pediatric
Crohn Disease Activity Index (PCDAI) analysis. Correlate the patient outcomes with the fecal
microbiome prior to, and after FMT.
STUDY SUBJECT INCLUSION CRITERIA:
Current IBD patients who have:
- UC patients with a flare due to failure of current therapy and have to undergo
esophagogastroduodenoscopy (EGD) and colonoscopy for restaging the disease and
escalation of therapy.
- CD patients with ileo colonic or colonic disease who require an EGD and colonoscopy
for disease assessment due to a flare or poor control.
- The ability to safely undergo colonoscopy (physical status classification used by the
American Society of Anesthesiologists).
- PUCAI score less than sixty five.
- PCDAI score less than forty.
STUDY SUBJECTS EXCLUSION CRITERIA:
- Patients with Crohn's disease: complications like an abscess, phlegmon, stricture,
small bowel obstruction, perforation, internal or external fistulization or infection
as causes for flare up before being deemed eligible for recruitment to the study. We
will check for these complications if a recent study has not been done.
- Severe immunosuppression: Biologicals with concomitant steroids (>30 mg/day).
- Central Line.
- Pressor or ventilatory support.
- On antibiotics.
- Patients with Crohn's disease found to have complications like an abscess, phlegmon,
stricture, small bowel obstruction, perforation, internal or external fistulization
or infection.
- Not willing to consent or follow guidelines throughout research trial.
- Screening labs in either donor or recipient reveal problems with performing fecal
microbiome transplantation because inclusion requirements are no longer met.
- Physician discretion.
- Participant request.
DONOR EXCLUSION CRITERIA:
- A history of antibiotic treatment during the 3 months preceding donation.
- A history of intrinsic gastrointestinal illnesses.
- A history of autoimmune or atopic illness or modulating therapy.
- A history of chronic pain syndromes, or neurologic or neurodevelopmental disorders.
- Metabolic syndrome or malnutrition or obesity.
- A history of exposure to infectious agents.
- Diarrhea or other symptoms of an intestinal infection within two weeks prior to, or
on the day of, stool donation.
- A history of malignant illnesses or ongoing oncologic therapy.
- Weight less than 15 kgs.
We found this trial at
1
site
4401 Penn Avenue
Pittsburgh, Pennsylvania 15224
Pittsburgh, Pennsylvania 15224
412-692-5325
Children's Hospital of Pittsburgh of UPMC UPMC is one of the leading nonprofit health systems...
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