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Biomarker-based Multidisciplinary Team (Bio-MDT) Approach to Personalized Microbial-targeted Treatment of Pouchitis and Crohn's Disease

Biomarker-based Multidisciplinary Team Approach to Personalized Microbial-targeted Treatment of Pouchitis and Crohn's Disease

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04082559
Acronym
Bio-MDT
Enrollment
170
Registered
2019-09-09
Start date
2019-06-11
Completion date
2023-06-11
Last updated
2020-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inflammatory Bowel Diseases

Keywords

IBD

Brief summary

Crohn's disease (CD) and ulcerative colitis (UC) are chronic inflammatory bowel diseases (IBD) currently affecting over 5 million patients globally, mostly young adults. These conditions are often debilitating, disabling and may markedly affect patient's quality of life. Despite important advances in research, the pathogenesis of IBD remains obscure, the incidence-rising, the condition - incurable, and drugs have a modest effect. The common denominator may be environmental factors, specifically diet and the microbiome, which remain a fundamental unmet need in IBD care as high quality randomized trials and mechanistic research are limited. Up to a quarter of patients with UC may undergo complete large bowel resection due to disease complications. In order to preserve bowel continuity, this surgery includes a restorative part with creation of a reservoir (pouch) from normal small bowel instead of the resected rectum. The majority of these patients develop small intestinal inflammation in the previously normal small bowel creating the pouch (pouchitis). Based on our results from previous studies, we hypothesized that personalized antibiotics and dietary interventions will modify microbial composition and result in significantly improved outcomes, specifically resolution of inflammation and prolonged remission rates in patients with a pouch. Aims: 1. Compare the effect of two antibiotic treatments on clinical, inflammatory and microbiological outcomes of patients with pouch inflammation. 2. Evaluate the effect of combined microbiome-targeted antibiotic and dietary intervention as treatment and prevention strategy in patients after pouch surgery. 3. Evaluate the effect of a microbiome-targeted dietary intervention as prevention strategy in patients after pouch surgery. 4. Identify predictors for response to specific antibiotic and dietary interventions.

Detailed description

All patients will undergo comprehensive screening by the bio-MDT. Aim 1: Antibiotic treatment- (patients with active disease) will be randomized to receive a prescription for one of two antibiotic regimens. 1. Ciprofloxacin + metronidazole 2. Doxycycline+ metronidazole Aim 2: Combination therapy ( Antibiotics+diet) After arm 1 recruitment completion, a favorable antibiotic regimen will be determined and recommended in arm 2, in which, patients with active disease will be randomized to 1. Favorable antibiotics + Mediterranean diet (MED) 2. Favorable antibiotics + The Specific Carbohydrate Diet (SCD) Aim 3: Nutritional prevention- Patients in clinical remission will be recruited to a dietary prevention study and be allocated to one of three groups: 1. Mediterranean diet (MED) 2. Control- based on the American Dietetic Association recommendations for patients with IBD. 3. Personalized nutrition group- based on prior results from study- NCT02858557 Comprehensive assessment including nutritional, clinical, inflammatory and microbial parameters will be performed at baseline and at weeks 2,3,4,8,26, 52.

Interventions

OTHERArm 1- Antibiotics treatment

Patients with active disease will be randomized and will receive a prescription antibiotic regimens

OTHERArm 2- Antibiotics treatment

Patients with active disease will be randomized and will receive a prescription antibiotic regimens

OTHERArm 1- Combination therapy (Antibiotics + diet)

Patients with active disease receiving a prescription for the antibiotic regimen defined as favorable in the antibiotics according to aim 1 , and randomized into one of two dietary interventions: Mediterranean diet (MED) or the specific carbohydrate diet (SCD).

OTHERArm 2- Combination therapy (Antibiotics + diet)

Patients with active disease receiving a prescription for the antibiotic regimen defined as favorable in the antibiotics according to aim 1 , and randomized into one of two dietary interventions: Mediterranean diet (MED) or the specific carbohydrate diet (SCD).

OTHERArm 1- Nutritional prevention

Patients in clinical remission will be recruited to a dietary prevention study

OTHERArm 2- Nutritional prevention

Patients in clinical remission will be recruited to a dietary prevention study

OTHERArm 3- Nutritional prevention

Patients in clinical remission will be recruited to a dietary prevention study

Sponsors

The Leona M. and Harry B. Helmsley Charitable Trust
CollaboratorOTHER
Tel Aviv University
CollaboratorOTHER
Rabin Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Patients are able and willing to sign an informed consent 2. Patients with UC who underwent pouch surgery and have a functioning pouch 3. Disease activity (PDAI and PGA) according to study arm 1-3 inclusion

Exclusion criteria

1. Patients with ileostomy 2. Significant comorbidity that precludes the patient from participating according to the physicians' judgment 3. Non-Hebrew readers 4. Pregnant and lactating women

Design outcomes

Primary

MeasureTime frameDescription
Time interval to responseOne yearDecrease in PGA and PDAI
Time interval to remissionOne yearPGA=0 and PDAI\<7

Countries

Israel

Contacts

Primary ContactIris Dotan, Prof
irisdo@clalit.org.il+97237525015
Backup ContactLihi Godny, BSc
lihigodny@gmail.com+97237525015

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026