The Crohn's Disease Exclusion Diet With Partial Enteral Nutrition or Alone in Adult Patients With Crohn's Disease (CDED-AD)
Primary Purpose
Crohn's Disease
Status
Completed
Phase
Not Applicable
Locations
Israel
Study Type
Interventional
Intervention
Crohns Disease Exclusion Diet + PEN
Crohns Disease Exclusion Diet
Sponsored by
About this trial
This is an interventional treatment trial for Crohn's Disease focused on measuring Crohn's disease, Mild to moderate Crohn's Disease, Diet, Enteral Nutrition
Eligibility Criteria
Inclusion Criteria
- Informed consent
- Established Crohn's disease
- Aged 18-55
- Duration of disease up to 5 years
- Harvey Bradshaw Index 5 ≤( HBI) ≤15
- Patients with uncomplicated disease involving the terminal ileum and or cecum
- Patients who performed colonoscopy (or MR/CTEnterography with elevated calprotectin>200) demonstrating active disease in the previous 8 weeks
Exclusion Criteria
- Patients with severe Disease (HBI > 15) or HBI<5
- Pregnancy,
- Patients with active extraintestinal disease, current B2 (Fixed non inflammatory stricture1 or small bowel obstruction) or B3 disease,
- Patients who used immunomodulator <8 weeks, or had dose changed in past 8 weeks,
- Patients with current or past use of biologics, or use of systemic steroids2,
- Patients with deep ulcers involving the colon distal to the splenic flexure on most recent colonoscopy
- Any proven current infection such as positive stool cultures or positive tests for parasites or C. difficile. Stool tests are mandatory only if diarrhea is present.
- Active Perianal disease ( clarification-fistula with discharge or abscess)
- Patients who have undergone an intestinal resection
- Patients with systemic disease including: type 2 diabetes, kidney failure, liver failure, neurological disease, active heart disease and patients with active autoimmune condition requiring medication3
- Patients unwilling to consume any animal source protein (eggs, chicken or fish).
Comments:
- Patients with ileo-cecal valve narrowing maybe included
- Patients active despite budesonide may enter the trial if they are on 3 mg, and stop budesonide within 14 days of commencement of the trial.
Patients with Celiac disease or Hashimoto Thyroiditis can be enrolled
-
Sites / Locations
- Haemek
- Wolfson Medical Center
- Rabin Medical Center
- Tel Aviv Sourasky Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Group 1
Group 2
Arm Description
Crohn's Disease Exclusion Diet+Partial Enteral Nutrition (PEN): Crohns Disease Exclusion Diet + PEN
Crohn's Disease Exclusion Diet alone with a calcium supplement
Outcomes
Primary Outcome Measures
Clinical remission defined as Harvey Bradshaw Index (HBI)<5
Secondary Outcome Measures
Steroid free remission between groups
Mucosal healing
Changes in mean C-Reactive Protein (CRP)
Change in mean fecal calprotectin
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT02231814
Brief Title
The Crohn's Disease Exclusion Diet With Partial Enteral Nutrition or Alone in Adult Patients With Crohn's Disease
Acronym
CDED-AD
Official Title
Dietary Therapy Using the Crohn's Disease Exclusion Diet (CDED) With Partial Enteral Nutrition or Alone for Induction and Maintenance of Remission in in Adults With Mild to Moderate Crohn's Disease- A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
December 2016 (Actual)
Primary Completion Date
December 2020 (Actual)
Study Completion Date
December 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Prof. Arie Levine
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will evaluate a novel diet for adult crohn's disease patients (The Crohn's Disease Exclusion Diet - CDED). Half of the patients in this study will receive the CDED alone while the other half will receive the CDED and a liquid diet formula, for 24 weeks.
Detailed Description
Environmental factors, the microbiome (bacteria in our gut) and innate immunity all play a role in the pathogenesis of Crohn's disease .Exclusive enteral nutrition (EEN) was found to be effective for inducing remission in active pediatric Crohn's disease, while Partial Enteral Nutrition (PEN) with free diet was not; suggesting that the mechanism of EEN depends on exclusion of dietary components. Dietary factors may play a role in the pathogenesis of the disease, and maybe an important under-investigated therapeutic target.
"The Crohn's Disease Exclusion Diet" (CDED) is a palatable diet excluding components suspected to interfere with the bacteria in our gut or impair immune mechanisms. Our group previously evaluated 47 patients using the Crohn's disease Exclusion Diet + 50% Polymeric formula for 6 weeks, and demonstrated a 78% response rate and 70% disease remission rate using stringent criteria. This was accompanied by a highly significant reduction in markers for inflammation (C-reactive protein (CRP) and Erythrocyte Sedimentation Rate (ESR)), and normalization of CRP in 70% of those entering remission. Among these patients were 13 adults aged 19-32, the remission rate in these 13 patients was 69%, similar to the pediatric data. Importantly, 6/7 patients in this study who refused to drink formula and just used the diet achieved remission, suggesting that the exclusion and not partial enteral nutrition are responsible for the high remission rate. Our former study did not evaluate mucosal healing as an end point, since performing colonoscopies after 6- 12 weeks of therapy is neither ethical nor feasible in children.
At present, data about nutritional therapy and this new dietary approach have been generated primarily in children, and this new diet has not been evaluated for early mucosal healing. The objectives of this pilot study are to generate data in adults, evaluate the diet over a longer period of time (24 weeks) and evaluate mucosal healing. The study is a prospective open label randomized controlled pilot trial in adults, with mild to moderate Crohn's disease who will receive the Crohn's Disease Exclusion Diet (CDED) for 24 weeks.
If effective, this could enable use of a feasible, safe intervention for induction and maintenance of remission as a new therapy or as an adjunctive therapy with medical therapy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Crohn's Disease
Keywords
Crohn's disease, Mild to moderate Crohn's Disease, Diet, Enteral Nutrition
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group 1
Arm Type
Experimental
Arm Description
Crohn's Disease Exclusion Diet+Partial Enteral Nutrition (PEN): Crohns Disease Exclusion Diet + PEN
Arm Title
Group 2
Arm Type
Experimental
Arm Description
Crohn's Disease Exclusion Diet alone with a calcium supplement
Intervention Type
Dietary Supplement
Intervention Name(s)
Crohns Disease Exclusion Diet + PEN
Other Intervention Name(s)
CDED + Liquid dietary formula
Intervention Description
Patients will use the CDED for a 24 week period, coupled with 1000 m"l of polymeric formula (1 Kcal/m"L) for the first 6 weeks. For weeks 7 to 24 patients will use the CDED coupled with 600 ml formula and a calcium supplement. The CDED is divided into 3 stages: 0-6 weeks induction phase, weeks 7-12 step down phase, weeks 13-24 maintenance phase.
Intervention Type
Other
Intervention Name(s)
Crohns Disease Exclusion Diet
Other Intervention Name(s)
CDED
Intervention Description
Crohn's Disease Exclusion Diet alone with a calcium supplement during the study (0-24). The CDED is divided into 3 stages: 0-6 weeks induction phase, weeks 7-12 step down phase, weeks 13-24 maintenance phase.
Primary Outcome Measure Information:
Title
Clinical remission defined as Harvey Bradshaw Index (HBI)<5
Time Frame
Week 6
Secondary Outcome Measure Information:
Title
Steroid free remission between groups
Time Frame
Week 6, 12 and 24.
Title
Mucosal healing
Time Frame
Week 24-26
Title
Changes in mean C-Reactive Protein (CRP)
Time Frame
Weeks 6, 12 and 24.
Title
Change in mean fecal calprotectin
Time Frame
Week 6, 12 and 24
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria
Informed consent
Established Crohn's disease
Aged 18-55
Duration of disease up to 5 years
Harvey Bradshaw Index 5 ≤( HBI) ≤15
Patients with uncomplicated disease involving the terminal ileum and or cecum
Patients who performed colonoscopy (or MR/CTEnterography with elevated calprotectin>200) demonstrating active disease in the previous 8 weeks
Exclusion Criteria
Patients with severe Disease (HBI > 15) or HBI<5
Pregnancy,
Patients with active extraintestinal disease, current B2 (Fixed non inflammatory stricture1 or small bowel obstruction) or B3 disease,
Patients who used immunomodulator <8 weeks, or had dose changed in past 8 weeks,
Patients with current or past use of biologics, or use of systemic steroids2,
Patients with deep ulcers involving the colon distal to the splenic flexure on most recent colonoscopy
Any proven current infection such as positive stool cultures or positive tests for parasites or C. difficile. Stool tests are mandatory only if diarrhea is present.
Active Perianal disease ( clarification-fistula with discharge or abscess)
Patients who have undergone an intestinal resection
Patients with systemic disease including: type 2 diabetes, kidney failure, liver failure, neurological disease, active heart disease and patients with active autoimmune condition requiring medication3
Patients unwilling to consume any animal source protein (eggs, chicken or fish).
Comments:
Patients with ileo-cecal valve narrowing maybe included
Patients active despite budesonide may enter the trial if they are on 3 mg, and stop budesonide within 14 days of commencement of the trial.
Patients with Celiac disease or Hashimoto Thyroiditis can be enrolled
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arie Levine, MD
Organizational Affiliation
Wolfson Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Iris Dotan, MD
Organizational Affiliation
Tel Aviv Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Irit Hermesh, MD
Organizational Affiliation
Rambam Medical Center,Haifa
Official's Role
Principal Investigator
Facility Information:
Facility Name
Haemek
City
Afula
Country
Israel
Facility Name
Wolfson Medical Center
City
Holon
Country
Israel
Facility Name
Rabin Medical Center
City
Petach Tikva
Country
Israel
Facility Name
Tel Aviv Sourasky Medical Center
City
Tel Aviv
Country
Israel
12. IPD Sharing Statement
Citations:
PubMed Identifier
24983973
Citation
Sigall-Boneh R, Pfeffer-Gik T, Segal I, Zangen T, Boaz M, Levine A. Partial enteral nutrition with a Crohn's disease exclusion diet is effective for induction of remission in children and young adults with Crohn's disease. Inflamm Bowel Dis. 2014 Aug;20(8):1353-60. doi: 10.1097/MIB.0000000000000110.
Results Reference
background
PubMed Identifier
34739863
Citation
Yanai H, Levine A, Hirsch A, Boneh RS, Kopylov U, Eran HB, Cohen NA, Ron Y, Goren I, Leibovitzh H, Wardi J, Zittan E, Ziv-Baran T, Abramas L, Fliss-Isakov N, Raykhel B, Gik TP, Dotan I, Maharshak N. The Crohn's disease exclusion diet for induction and maintenance of remission in adults with mild-to-moderate Crohn's disease (CDED-AD): an open-label, pilot, randomised trial. Lancet Gastroenterol Hepatol. 2022 Jan;7(1):49-59. doi: 10.1016/S2468-1253(21)00299-5. Epub 2021 Nov 2.
Results Reference
background
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The Crohn's Disease Exclusion Diet With Partial Enteral Nutrition or Alone in Adult Patients With Crohn's Disease
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