Fecal Microbiota Transplantation (FMT) for Treatment of Ulcerative Colitis in Children

Sponsor

Baylor College of Medicine (Other)

Overall Status

Completed

CT.gov ID

NCT01947101

Collaborator

(none)

Enrollment

Location

Arm

26.9

Duration (Months)

0.2

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Patients diagnosed with ulcerative colitis (UC), a specific type of inflammatory bowel disease, will be invited to take part in this study. The investigators do not know what causes UC. However, the microbes (such as bacteria and viruses), which normally live in our intestines are thought to play an important role in the development of UC. There are many treatment options for UC such as steroids,and other medications that decrease inflammation. However, none of these can cure the disease.

This study aims to treat pediatric UC in an alternative fashion by changing the microbes in the gut by giving the participant's stool specimens from healthy adult individuals. There is some evidence from a few cases of adult UC that this therapy may cure the disease or at least provide long lasting suppression (remission) of the symptoms. The investigators would like to test this therapeutic intervention in children with UC.

The purpose of this study is to (1) examine the microbiome of stool and colon (2) and to determine whether healthy-donated stool enemas can treat pediatric ulcerative colitis. (3) The investigators will also study the effects of the treatment on colonic gene expression.

Condition or Disease	Intervention/Treatment	Phase
Ulcerative Colitis	Biological: Fecal Microbiota Transplant	Phase 1

Detailed Description

FMT RECIPIENTS:

Participants will be recruited from the patient population treated by the Pediatric Gastroenterology, Hepatology, and Nutrition Section at Baylor College of Medicine/Texas Children's Hospital.

I. Activities prior to starting FMT therapy:

Participants will be asked to discontinue or taper their current home medications for ulcerative colitis.
Participants will be asked to complete enema training.
The participant and family will be counseled in case emergency surgical and/or intensive care interventions are required.
Survey Completion to assess clinical symptoms.

II. Initiation of FMT Therapy:

Pre-colonoscopy and FMT therapy preparation:

One to two days prior to scheduled colonoscopy the study participant will be asked to provide a stool sample. They will also undergo a bowel clean-out with Miralax for colonoscopy preparation. Colonoscopy (endoscopic examination of the large bowel) will be used to deliver the first donor fecal transplant at the beginning of the therapeutic protocol.

FMT treatment and Initial colonoscopy:

Fecal microbiota transplantation is made possible by utilizing a donor (healthy adult) providing their stool sample. The donor's stool will be screened and tested for known disease-causing agents including viruses, bacteria and parasites to prevent spread of disease to the participant.

On the first day of treatment, the participant will undergo a colonoscopy to deliver the filtered donor stool directly into their colon. Additionally, biopsies will be taken during this procedure for routine diagnostic as well as research purposes.

III. Subsequent FMT treatments:

Enemas will be given periodically to complete a total of 1-year therapy.

IV. Follow-up endoscopy and samples:

A similar but more limited procedure (sigmoidoscopy) will be repeated at 14 weeks into the study period. Biopsies will be taken during this procedure for routine diagnostic as well as research purposes.

FMT DONORS:

Potential healthy adult stool donors (between 18 and 45 years of age) will be recruited by the research staff. They will be asked to volunteer for the screening and regularly supply stool samples according to the study protocol.

Study Design

Study Type:

Interventional

Actual Enrollment :

6 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase I Study of Fecal Microbiota Transplantation (FMT) in Immunomodulator Dependent Pediatric Ulcerative Colitis (UC)

Study Start Date :

Feb 1, 2014

Actual Primary Completion Date :

Dec 1, 2014

Actual Study Completion Date :

May 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Ulcerative Colitis Fecal Microbiota Transplant	Biological: Fecal Microbiota Transplant Fecal Microbiota Transplant will be endoscopically administered directly into the colon. Consecutive treatments will be given by rectal enema route. Other Names: stool transplant

Arm

Intervention/Treatment

Experimental: Ulcerative Colitis

Fecal Microbiota Transplant

Biological: Fecal Microbiota Transplant

Fecal Microbiota Transplant will be endoscopically administered directly into the colon. Consecutive treatments will be given by rectal enema route.

Other Names:

stool transplant

Outcome Measures

Primary Outcome Measures

Assess safety of FMT treatment by recording the frequency of adverse events. [12 months]
To determine the safety and associated toxicities of serial FMTs in pediatric UC following withdrawal from standard therapy.

Secondary Outcome Measures

Assess efficacy of FMT treatment with the aid of the Pediatric Ulcerative Colitis Activity (PUCAI) Index, a validated measure of clinical disease severity. [1 year]
To preliminarily assess the efficacy of FMT in inducing or maintaining clinical remission of UC.

Eligibility Criteria

Criteria

Ages Eligible for Study:

12 Years to 20 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Yes

Patient Inclusion Criteria:

Patients must have a diagnosis of ulcerative colitis based on clinical symptoms, as well as laboratory and colonoscopic findings, including histopathologic results of the intestinal mucosa.
Pediatric Ulcerative Colitis Activity Index (PUCAI) < 35 [mild activity] as assessed within 4 weeks prior to enrollment and clinical symptoms that are at least stable.
Patients must be "immunomodulator dependent," i.e., have a history of steroid dependency (lack of clinical remission for over 8 weeks without steroid therapy), and/or being immunomodulator (azathioprine, 6-mercaptopurine, methotrexate, etc.) treated, and/or biologic agent (infliximab, adalimumab, etc.) treated
Patients ≥ 12 and < 21 years of age are eligible for this trial.
Patients must be willing to be off current UC therapies.
Willingness to undergo a surgical consultation prior to FMT treatment.
Patients who are not enema trained will be required to undergo enema training prior to the start of FMT treatment.
All patients and/or their parents or legally authorized representatives must sign a written informed consent document. Assent, when appropriate, will be obtained according to institutional guidelines.

Patient Exclusion Criteria:

Patients who are known to have the following will be excluded:

Decompensated liver cirrhosis (bleeding varices, ascites, encephalopathy or icterus)
Human immunodeficiency virus (HIV)/acquired immune deficiency syndrome (AIDS)
Bone marrow transplantation within the past 150 days
Other severe immunodeficiency

Patients with severe prior allergic reaction to food will be excluded from the protocol.
Patients who are pregnant or lactating will be excluded from the protocol.