Inflammatory Bowel DiseasePhase 1FMT IBDNCT02391012
Fecal Transplantation for Inflammatory Bowel Disease
A Phase 1 study testing Fecal microbial l transplantation in people with Inflammatory Bowel Disease, run by Meir Medical Center at 2 sites in Israel.
Trial summary
Fecal microbial treatment (FMT) is a treatment that utilizes the microbiota of a healthy intestine as a probiotic preparation. The feces of a healthy individual is fluidized and than inserted into the intestinal tract of a sick individual, assuming that the healthy flora will colonize and cure the intestine. Read more about this study
- Who is it for?
- Ages 18 to 80 years
- Conditions the study is for
- Inflammatory Bowel Disease
- What is being tested?
- Fecal microbial l transplantation
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 9 participants
- Where
- 2 sitesIsrael
- Study dates
- Apr 2015to Jul 2016
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Signed informed consent
- Inflammatory bowel disease diagnosed at least 3 months ago
- Failure of either one immunomodulator of at least 3 months duration, or TNF inhibitor full induction treatment, or intolerance to either of these drugs.
- Currently active disease, partial Mayo score ≥4 for ulcerative colitis, or CDAI ≥200 for CD.
- negative HIV , HTLV I/II, negative stool culture, Negative C diff toxin, negative CMV
Who cannot join
- No informed consent
- Non active inflammatory bowel disease.
- Active infection in either the donor or the recipient,
Trial locations and contacts
2 sites in 1 country.
Israel2 sites
Meir hospital
Kfar Saba, 44281
Gastroenterology institute Meir Hospital
Kfar Saba
About this study
Fecal microbial treatment (FMT) is a treatment that utilizes the microbiota of a healthy intestine as a probiotic preparation. The feces of a healthy individual is fluidized and than inserted into the intestinal tract of a sick individual, assuming that the healthy flora will colonize and cure the intestine. There are reports of the efficacy of this treatment for inflammatory bowel disease but currently the numbers are small.
aim: To investigate whether use of FMT will bring improvement for colitis in IBD patients . Methods: The patients will undergo full colonoscopy, the stool preparation will be infused through the colonoscope during withdrawal of the instrument.
Read the detailed description
Back ground: intestinal microbiota have a central role in disease pathogenesis, either in a form of a "permissive" role or as a direct pathogenic cause.
Clostridium difficile colitis; irritable bowel syndrome (IBS) and IBD have all been connected to a disturbance in the equilibrium of intestinal microbiome. But the causative mechanism is not yet known. (5-10) . Various bacteria including lactobacillus acidophilus and bifidobacterium bifidus are being empirically used as treatment for many intestinal ailments. The cause of inflammatory bowel disease in unknown but evidence is gathering that excessive immune reaction of intestinal immune system to microflora combined with a genetic predisposition are responsible for the chronic inflammation.
Fecal microbial treatment (FMT) is a treatment that utilizes the microbiota of a healthy intestine as a probiotic preparation. The feces of a healthy individual is fluidized and that inserted into the intestinal tract of a sick individual, assuming that the healthy flora will colonize and cure the intestine. Previous work had shown success in fecal transplantation as a treatment for clostridium difficile colitis. There are also reports of the efficacy of this treatment for inflammatory bowel disease but currently the numbers are small. A review by Anderson et al describes 17 studies reporting treatment of IBD by FMT. (12). In 9 cases it was done to treat IBD and in 8 cases for intestinal infection in IBD patients. Altogether 41 cases were reported , In some the FMT was inserted through a nasogastric tube directly to the duodenum, in some be colonoscopy and in some by an enema. A significant clinical improvement was reported in 19/25 patients. 13/17 stopped IBD treatment , 15/24 entered full clinical remission. In all 15 patients treated for infection the treatment was successful. No sever adverse effects were reported, Fever was developed in 8 cases and in one case there was exacerbation of colitis after treatment.
Primary aim: To investigate whether use of FMT will bring improvement of at least 2 points in partial mayo score in ulcerative colitis patients, or 70 points in CDAI of patients with Crohn's colitis. One month after FMT.
Improvement will be defined as:
For Ulcerative colitis: a decrease of at least 2 points in the partial mayo score, and a decrease of at least 1 point in endoscopic Mayo score.
For Crohn's disease: A decrease of at least 70 points in Crohn's disease activity index (CDAI) .
Materials and methods:
Study population: 40 patients aged 18-80 years, with histological and endoscopic diagnosis of ulcerative colitis or crohn's colitis who did not respond to either thiopurines or tumor necrosis factor (TNF) inhibitors.
Exacerbation will be defined as partial mayo score higher then 3, with either CRP higher than 0.5 or endoscopic mayo score >1 in ulcerative colitis and CDAI higher them 220 and C reactive protein (CRP) higher than 0.5 in Crohn's colitis.
Stool will be donated by the patients choice either from a relative, preferably a partner to minimize possible transference of an infective agent, alternatively samples will be ordered from "open biom".
Endoscopic disease activity will be defined as follows:
Endoscopic Mayo score:
- Normal or inactive disease: 0
- Mild disease (erythema, decreased vascular pattern, mild friability): 1
- Moderate disease (marked erythema, absent vascular pattern, friability, erosions): 2
- Severe disease (spontaneous bleeding, ulceration): 3
Simple endoscopic score Crohns disease (SES-CD):
Segments of intestine: Rectum,Sigmoid and left colon, Transverse colon,Right colon, Ileum for each segment the Presence of: ulcers,Ulcerated surface, Affected surface, Presence of narrowing, and number of affected segments will be evaluated and the total score sumed, The SES-CD will than be calculated as follows: TOTAL - 1.4 X (number of affected segments) = E-CDI
Inclusion criteria
Donor:
- Signed informed consent
- Basically healthy, no hospitalization in the last 6 months, no active malignant disease (with the exclusion of Basal cell skin tumor that was treated).
- No antibiotic treatment in the last 6 months
- Preferably a partner of the patient, or a relative leaving in the same house
- No febrile illness in the last month
- Normal laboratory tests including: blood count, liver and kidney function, negative hepatitis A immunoglobulin M (IgM), negative hepatitis C antibody, negative HbsAg, negative HIV , human T-lymphotropic virus (HTLV I/II), negative venereal disease research laboratory ( VDRL).
- Stool tests: Negative stool culture, negative C. difficile toxins (A and B). Negative parasite microscopy. Fecal calprotectin.
Patient:
- Signed informed consent
- Inflammatory bowel disease diagnosed at least 3 months ago
- Failure of either one immunomodulator of at least 3 months duration, or TNF inhibitor full induction treatment, or intolerance to either of these drugs.
- Currently active disease, partial Mayo score ≥4 for ulcerative colitis (UC), or CDAI ≥200 for Crohn's disease (CD).
- negative HIV , HTLV I/II, negative stool culture, Negative C diff toxin, negative cytomegalovirus ( CMV)
Treatment protocol:
- Both donor and recipient will sign informed consent
- Both donor and recipient will do the above mentioned laboratory tests, the investigator will verify that the results are negative.
- Recipient will be prepared for colonoscopy with 3 liters of polyethylene glycol according to the routine protocol.
- The donor will bring same day stool, alternatively, preparation from "open biom" will be used.
- 200 gr stools will be mixed with sterile 200ml sodium chloride (NACL) 0.9% and then filtered to exclude large particles.
- The patients will undergo full colonoscopy, the stool preparation will be infused through the colonoscope during withdrawal of the instrument.
- If no improvement within 7 days, the patient will be offered the option of another FMT using enema prepared in a similar manner.
- Patients will be instructed to maintain a high fiber diet,
Follow up:
On first colonoscopy:
Exact description of the length of the involved segment + Mayo visual score for UC and simple endoscopic score - CD (SES -CD) for Crohn's disease.
2 biopsies from each colonic segment: Rt colon, transverse colon, left colon, rectum.
Weekly partial Mayo score or Harvey Bradshow Index (HBI ) in the first month, then once a month for 6 months.
After 6 months repeat colonoscopy + biopsies + stool samples. Colonoscopy does not have to be complete but has to include the segment that was inflamed in the first colonoscopy.
At the time of colonoscopy blood tests including complete blood count (CBC), liver and kidney function, CRP, fecal calprotectin.
Microbiota profiles:
- From both the donor and the recipient before FMT.
- From the recipient: one month and 6 months after FMT. Stool samples will be frozen immediately at -20° and then transferred to the laboratory for microbiota analysis.
- Conditions
- Inflammatory Bowel Disease
- Being tested
- Fecal microbial l transplantation
- Keywords
- Ulcerative colitis, Crohns disease, Microbial transplantation
- Medical subject headings
- Inflammatory Bowel Diseases, Colitis, Ulcerative, Crohn Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Fecal microbial l transplantationBiological
Also called FMT
infusion of preparation of fecal preparation from a healthy donor to a colitis patient
| Study group | Role | What they receive |
|---|---|---|
| Fecal microbial l transplantation | Experimental | patients with active colitis who will undergo treatment by fecal microbial transplantation Receives: Biological: Fecal microbial l transplantation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Improvement of disease activity index.
: a decrease of at least 2 points in the partial mayo score, and a decrease of at least 1 point in endoscopic Mayo score.
For Crohn's disease: A decrease of at least 70 points in CDAI.
Measured: 4 weeks
Secondary outcomes (5)
improvement of endoscopic score
Improvement of at least one point in endoscopic score
Measured: 4 weeks
Maintenance of remission/ improvement during follow up
Maintenance of remission/ improvement during follow up
Measured: 6 months
Patients perspective of the treatment (do patients regard the treatment as acceptable)
do patients regard the treatment as acceptable
Measured: 6 months
Cost estimation of the treatment
cost of treatment
Measured: 6 months
side effects (presence of fever,or rise of 50% or more in the number of bowel movements)
monitoring side effects of treatment,specifically the presence of fever above 38ۨ c or a rise of 50% or more in the number of bowel movements during the first 3 days after the infusion
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Mar 2015 (estimated)
- Study startApr 2015
- Primary completionJun 2016
- Study completionJul 2016 (estimated)
Why it stopped: unable to recruit enough patients
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Inflammatory Bowel DiseaseStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Enrolment
- 9 participants (actual)
Sponsor and investigators
- Lead sponsor
- Meir Medical Center
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, NAFTALI TIMNA, Meir Medical Center
- Investigators
- Timna Naftali, MD, Principal investigator, Meir Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02391012
- Sponsor's protocol ID
- 0198-12-MMC
- Acronym
- FMT IBD
- Status last verified
- Jun 2016
- First submitted
- 5 Mar 2015
- Last updated
- 14 Jun 2016
- Results posted
- No
- Data monitoring committee
- No
Publications
Anderson JL, Edney RJ, Whelan K. Systematic review: faecal microbiota transplantation in the management of inflammatory bowel disease. Aliment Pharmacol Ther. 2012 Sep;36(6):503-16. doi: 10.1111/j.1365-2036.2012.05220.x. Epub 2012 Jul 25.
PubMed 22827693
Study at a glance
From the registry record, last updated by the sponsor on 14 Jun 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Fecal Transplantation for Inflammatory Bowel Disease
- ClinicalTrials.gov ID
- NCT02391012
- Acronym / sponsor ID
- FMT IBD / 0198-12-MMC
- Conditions
- Inflammatory Bowel Disease
- Keywords
- Ulcerative colitis, Crohns disease, Microbial transplantation
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: unable to recruit enough patients
- Enrolment
- 9 participants (actual)
- Lead sponsor
- Meir Medical CenterUniversity, hospital or other
- Study start
- Apr 2015
- Primary completion
- Jun 2016 (actual)
- Study completion
- Jul 2016 (estimated)
- First posted
- 18 Mar 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Fecal microbial treatment (FMT) is a treatment that utilizes the microbiota of a healthy intestine as a probiotic preparation. The feces of a healthy individual is fluidized and than inserted into the intestinal tract of a sick individual, assuming that the healthy flora will colonize and cure the intestine. There are reports of the efficacy of this treatment for inflammatory bowel disease but currently the numbers are small.
aim: To investigate whether use of FMT will bring improvement for colitis in IBD patients . Methods: The patients will undergo full colonoscopy, the stool preparation will be infused through the colonoscope during withdrawal of the instrument.
Detailed description
Back ground: intestinal microbiota have a central role in disease pathogenesis, either in a form of a "permissive" role or as a direct pathogenic cause.
Clostridium difficile colitis; irritable bowel syndrome (IBS) and IBD have all been connected to a disturbance in the equilibrium of intestinal microbiome. But the causative mechanism is not yet known. (5-10) . Various bacteria including lactobacillus acidophilus and bifidobacterium bifidus are being empirically used as treatment for many intestinal ailments. The cause of inflammatory bowel disease in unknown but evidence is gathering that excessive immune reaction of intestinal immune system to microflora combined with a genetic predisposition are responsible for the chronic inflammation.
Fecal microbial treatment (FMT) is a treatment that utilizes the microbiota of a healthy intestine as a probiotic preparation. The feces of a healthy individual is fluidized and that inserted into the intestinal tract of a sick individual, assuming that the healthy flora will colonize and cure the intestine. Previous work had shown success in fecal transplantation as a treatment for clostridium difficile colitis. There are also reports of the efficacy of this treatment for inflammatory bowel disease but currently the numbers are small. A review by Anderson et al describes 17 studies reporting treatment of IBD by FMT. (12). In 9 cases it was done to treat IBD and in 8 cases for intestinal infection in IBD patients. Altogether 41 cases were reported , In some the FMT was inserted through a nasogastric tube directly to the duodenum, in some be colonoscopy and in some by an enema. A significant clinical improvement was reported in 19/25 patients. 13/17 stopped IBD treatment , 15/24 entered full clinical remission. In all 15 patients treated for infection the treatment was successful. No sever adverse effects were reported, Fever was developed in 8 cases and in one case there was exacerbation of colitis after treatment.
Primary aim: To investigate whether use of FMT will bring improvement of at least 2 points in partial mayo score in ulcerative colitis patients, or 70 points in CDAI of patients with Crohn's colitis. One month after FMT.
Improvement will be defined as:
For Ulcerative colitis: a decrease of at least 2 points in the partial mayo score, and a decrease of at least 1 point in endoscopic Mayo score.
For Crohn's disease: A decrease of at least 70 points in Crohn's disease activity index (CDAI) .
Materials and methods:
Study population: 40 patients aged 18-80 years, with histological and endoscopic diagnosis of ulcerative colitis or crohn's colitis who did not respond to either thiopurines or tumor necrosis factor (TNF) inhibitors.
Exacerbation will be defined as partial mayo score higher then 3, with either CRP higher than 0.5 or endoscopic mayo score >1 in ulcerative colitis and CDAI higher them 220 and C reactive protein (CRP) higher than 0.5 in Crohn's colitis.
Stool will be donated by the patients choice either from a relative, preferably a partner to minimize possible transference of an infective agent, alternatively samples will be ordered from "open biom".
Endoscopic disease activity will be defined as follows:
Endoscopic Mayo score:
- Normal or inactive disease: 0
- Mild disease (erythema, decreased vascular pattern, mild friability): 1
- Moderate disease (marked erythema, absent vascular pattern, friability, erosions): 2
- Severe disease (spontaneous bleeding, ulceration): 3
Simple endoscopic score Crohns disease (SES-CD):
Segments of intestine: Rectum,Sigmoid and left colon, Transverse colon,Right colon, Ileum for each segment the Presence of: ulcers,Ulcerated surface, Affected surface, Presence of narrowing, and number of affected segments will be evaluated and the total score sumed, The SES-CD will than be calculated as follows: TOTAL - 1.4 X (number of affected segments) = E-CDI
Inclusion criteria
Donor:
- Signed informed consent
- Basically healthy, no hospitalization in the last 6 months, no active malignant disease (with the exclusion of Basal cell skin tumor that was treated).
- No antibiotic treatment in the last 6 months
- Preferably a partner of the patient, or a relative leaving in the same house
- No febrile illness in the last month
- Normal laboratory tests including: blood count, liver and kidney function, negative hepatitis A immunoglobulin M (IgM), negative hepatitis C antibody, negative HbsAg, negative HIV , human T-lymphotropic virus (HTLV I/II), negative venereal disease research laboratory ( VDRL).
- Stool tests: Negative stool culture, negative C. difficile toxins (A and B). Negative parasite microscopy. Fecal calprotectin.
Patient:
- Signed informed consent
- Inflammatory bowel disease diagnosed at least 3 months ago
- Failure of either one immunomodulator of at least 3 months duration, or TNF inhibitor full induction treatment, or intolerance to either of these drugs.
- Currently active disease, partial Mayo score ≥4 for ulcerative colitis (UC), or CDAI ≥200 for Crohn's disease (CD).
- negative HIV , HTLV I/II, negative stool culture, Negative C diff toxin, negative cytomegalovirus ( CMV)
Treatment protocol:
- Both donor and recipient will sign informed consent
- Both donor and recipient will do the above mentioned laboratory tests, the investigator will verify that the results are negative.
- Recipient will be prepared for colonoscopy with 3 liters of polyethylene glycol according to the routine protocol.
- The donor will bring same day stool, alternatively, preparation from "open biom" will be used.
- 200 gr stools will be mixed with sterile 200ml sodium chloride (NACL) 0.9% and then filtered to exclude large particles.
- The patients will undergo full colonoscopy, the stool preparation will be infused through the colonoscope during withdrawal of the instrument.
- If no improvement within 7 days, the patient will be offered the option of another FMT using enema prepared in a similar manner.
- Patients will be instructed to maintain a high fiber diet,
Follow up:
On first colonoscopy:
Exact description of the length of the involved segment + Mayo visual score for UC and simple endoscopic score - CD (SES -CD) for Crohn's disease.
2 biopsies from each colonic segment: Rt colon, transverse colon, left colon, rectum.
Weekly partial Mayo score or Harvey Bradshow Index (HBI ) in the first month, then once a month for 6 months.
After 6 months repeat colonoscopy + biopsies + stool samples. Colonoscopy does not have to be complete but has to include the segment that was inflamed in the first colonoscopy.
At the time of colonoscopy blood tests including complete blood count (CBC), liver and kidney function, CRP, fecal calprotectin.
Microbiota profiles:
- From both the donor and the recipient before FMT.
- From the recipient: one month and 6 months after FMT. Stool samples will be frozen immediately at -20° and then transferred to the laboratory for microbiota analysis.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Fecal microbial l transplantation | Experimental | Biological: Fecal microbial l transplantationpatients with active colitis who will undergo treatment by fecal microbial transplantation |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- Signed informed consent
- Inflammatory bowel disease diagnosed at least 3 months ago
- Failure of either one immunomodulator of at least 3 months duration, or TNF inhibitor full induction treatment, or intolerance to either of these drugs.
- Currently active disease, partial Mayo score ≥4 for ulcerative colitis, or CDAI ≥200 for CD.
- negative HIV , HTLV I/II, negative stool culture, Negative C diff toxin, negative CMV
Key exclusion criteria (3 listed)
- No informed consent
- Non active inflammatory bowel disease.
- Active infection in either the donor or the recipient,
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Fecal microbial l transplantationAlso: FMTinfusion of preparation of fecal preparation from a healthy donor to a colitis patient | Biological | Fecal microbial l transplantation |
Primary outcome
Improvement of disease activity index.
Time frame: 4 weeks
: a decrease of at least 2 points in the partial mayo score, and a decrease of at least 1 point in endoscopic Mayo score. For Crohn's disease: A decrease of at least 70 points in CDAI.
5 secondary outcomes
improvement of endoscopic score
Time frame: 4 weeks
Maintenance of remission/ improvement during follow up
Time frame: 6 months
Patients perspective of the treatment (do patients regard the treatment as acceptable)
Time frame: 6 months
Cost estimation of the treatment
Time frame: 6 months
side effects (presence of fever,or rise of 50% or more in the number of bowel movements)
Time frame: 6 months
Results and safety
The study was stopped early (reason given: unable to recruit enough patients). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 14 Jun 2016.
- Background: PubMed 22827693Anderson JL, Edney RJ, Whelan K. Systematic review: faecal microbiota transplantation in the management of inflammatory bowel disease. Aliment Pharmacol Ther. 2012 Sep;36(6):503-16. doi: 10.1111/j.1365-2036.2012.05220.x. Epub 2012 Jul 25.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Timna Naftali, MD principal investigator
Meir Medical Center
2 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing Fecal microbial l transplantation in people with Inflammatory Bowel Disease, run by Meir Medical Center at 2 sites in Israel.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: stopped early, as of the sponsor's last update on 14 Jun 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 2 sites in Israel. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: unable to recruit enough patients). Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Improvement of disease activity index. (time frame: 4 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02391012, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 14 Jun 2016.