DIETOMICS-CD: Diet for Induction and Maintenance of Remission and Re-biosis in Crohn's Disease

Sponsor
Prof. Arie Levine (Other)
Overall Status
Completed
CT.gov ID
NCT02843100
Collaborator
(none)
63
7
2
49.6
9
0.2

Study Details

Study Description

Brief Summary

The modified-Exclusive Enteral Nutrition (mEEN) is an open label randomized controlled trial in mild to severe Crohn's Disease patients. The purpose of this study is to determine whether induction of remission and maintenance of remission can be achieved with a new dietary strategy that involves only 2 weeks of Exclusive Enteral Nutrition (EEN) with Modulen and 12 weeks of an exclusion diet involving selected table foods. This novel approach will be compared to the gold standard dietary regime involving 8 weeks of EEN.

Condition or Disease Intervention/Treatment Phase
  • Other: Modified Exclusive Enteral Nutrition
  • Other: Crohn's Disease Exclusion Diet
  • Other: Partial Enteral Nutrition
  • Other: Standard Exclusive Enteral Nutrition
N/A

Detailed Description

Rational: Exclusive enteral nutrition (EEN) is an established but difficult to perform method for induction of remission and cannot be used for maintenance of remission. It entails drinking only liquid formula for 8 weeks. Refusal to use or to adhere to this therapy is not uncommon and leads to use of other non- dietary strategies in children including steroids and immunosuppression. The Crohn's Disease Exclusion Diet (CDED) with partial enteral nutrition has been shown to be effective for children with mild to moderate disease. The investigators have developed a maintenance strategy using the CDED.

Objectives: To prove that induction of remission and maintenance of remission can be achieved with a new dietary strategy that involves only 2 weeks of EEN with Modulen and 12 weeks of an exclusion diet involving selected table foods.

Methods: Open label randomized controlled pilot trial comparing two weeks of EEN followed by the CDED and Partial Enteral Nutrition (PEN), to 8 weeks of EEN followed by PEN with free diet. The study will include a control group of healthy children for microbiome studies.

Population: Age 8-18 years with mild to severe active Crohn's disease defined as 15≤Pediatric Crohn's Disease Activity Index (PCDAI)<47.5.

Time frame: The induction of remission phase will last 8 weeks followed by maintenance phase for a period of 24 weeks.

Expected outcomes and significance: If this method proves to be equivalent to EEN, the duration of use of EEN will be only two weeks, allowing more patients access to dietary therapy. More importantly, this study will also evaluate two maintenance strategies and will be the first to evaluate re-biosis.

Study Design

Study Type:
Interventional
Actual Enrollment :
63 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Modified Exclusive Enteral Nutrition With the Crohn's Disease Exclusion Diet for Induction and Maintenance of Remission and Re-biosis
Actual Study Start Date :
Apr 10, 2018
Actual Primary Completion Date :
May 29, 2022
Actual Study Completion Date :
May 29, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group 1

Modified Exclusive Enteral Nutrition including two weeks of Exclusive Enteral Nutrition (EEN) using Modulen followed by Partial Enteral Nutrition (PEN) along with the Crohn's Disease Exclusion Diet (CDED) phases 2 & 3 for 24 weeks

Other: Modified Exclusive Enteral Nutrition
Two weeks of Exclusive Enteral Nutrition with Modulen
Other Names:
  • Modulen, Nestle
  • Other: Crohn's Disease Exclusion Diet
    a limited whole food diet
    Other Names:
  • CDED
  • Other: Partial Enteral Nutrition
    25-50% of Energy from formula
    Other Names:
  • Modulen, Nestle
  • Active Comparator: Group 2

    Standard Exclusive Enteral Nutrition for 8 weeks using Modulen, followed by free diet with gradual reduction of Modulen to 25% of energy needs by week 24.

    Other: Partial Enteral Nutrition
    25-50% of Energy from formula
    Other Names:
  • Modulen, Nestle
  • Other: Standard Exclusive Enteral Nutrition
    8 weeks of Exclusive Enteral Nutrition
    Other Names:
  • Modulen, Nestle
  • Outcome Measures

    Primary Outcome Measures

    1. ITT, steroid free Clinical remission (defined as Pediatric Crohn's Disease Activity Index (PCDAI)<10) at week 14 [week 14]

      Sustained remission with EEN Vs CDED+PEN

    Secondary Outcome Measures

    1. ITT steroid free remission at week 8 [week 8]

      Induction of remission

    2. Microbiome composition difference between groups at week 14 [week 14]

      Assessment of microbiome composition and metabolomics

    3. 3. Reduction of at least 50% from baseline in fecal calprotectin at week 24 for patients on original treatment [week 24]

      Mucosal healing assessment

    4. Steroid and biologic free sustained remission at week 24. [week 14 and 24]

      Remission achieved and maintained without additional therapy

    5. Need for additional treatment to achieve remission by week 14 [Week 14]

      Remission achieved without additional therapy

    6. Mucosal healing as assessed by MRE in dietary responsive disease at week 52 [Week 52]

      Mucosal healing

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    8 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion criteria:
    1. Established diagnosis of Crohn's disease.

    2. Patients with mild to severe active Crohn's disease (15≤PCDAI≤47.5)

    3. Ages 8-18

    4. Duration of disease ≤ 36 months

    5. Active inflammation (CRP≥>0.6 mg /dL or ESR≥>20 or Calprotectin≥>200 mcg/gr within the past 3 weeks) during screening

    6. Patients with B1, P0 uncomplicated disease at enrollment

    7. Patients with disease defined as L1, L4, L3 or L2 limited to cecum, ascending or transverse colon or L2 with left sided disease with terminal ileum or small bowel involvement in the past by the Paris classification (patients with macroscopic disease)

    8. Signed informed consent

    Exclusion Criteria:
    1. Patients with very mild disease (PCDAI 12.5 -15) or very severe disease (PCDAI >47.5)

    2. Pregnancy

    3. Patients who have disease confined to the colon involving the descending colon, rectum or sigmoid colon and no prior history of small bowel involvement

    4. Patients who have active extra intestinal disease (such as Arthritis, Uveitis, Pyoderma Gangrenosum, Erythema Nodosum etc.)

    5. Patients with complicated disease (B2, B3)

    6. Patients who recently onset use of an immunomodulator <8 weeks, or dose change in past 8 weeks.

    7. Patients with current use of biologics, or use in last 8 weeks or current use of systemic steroids

    8. Patients who have active perianal disease ( active fistula or abscess)

    9. Patients who have positive stool cultures with relevant pathogens,, or positive tests for parasites or C. difficile. Stool tests are mandatory only if diarrhea is present.

    10. Patients with fever > 38.3

    11. Documented milk protein allergy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Dr. Eytan Wine, Edmonton Canada
    2 Johan Van Limbergen Halifax Canada
    3 Dr Sally Lawrence Vancouver Canada
    4 Dr. Séamus Hussey Dublin Ireland
    5 The E. Wolfson.Medical Center Holon Israel 58100
    6 Dr. Francisco Javier Martin Carpi Barcelona Spain
    7 Dr. Víctor Manuel Navas López Málaga Spain

    Sponsors and Collaborators

    • Prof. Arie Levine

    Investigators

    • Principal Investigator: Rotem Sigall Boneh, RD, Pediatric Gastroenterology and Nutrition unit; The E. Wolfson.Medical Center
    • Study Director: Michal Yaakov, Pediatric Gastroenterology and Nutrition unit; The E. Wolfson.Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Prof. Arie Levine, Director, Pediatric Gastroenterology and Nutrition unit, Wolfson Medical Center
    ClinicalTrials.gov Identifier:
    NCT02843100
    Other Study ID Numbers:
    • 0075-16 WOMC
    First Posted:
    Jul 25, 2016
    Last Update Posted:
    Jun 1, 2022
    Last Verified:
    May 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Prof. Arie Levine, Director, Pediatric Gastroenterology and Nutrition unit, Wolfson Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jun 1, 2022