Partial Enteral Nutrition With a Unique Diet vs. Exclusive Enteral Nutrition for the Treatment of Pediatric Crohn's Disease

Not Applicable

Completed

• Conditions: Crohn's Disease
• Interventions: Other: Unique Diet+Partial Enteral Nutrition; Other: Exclusive Enteral Nutrition (Modulen)

• Registration Number: NCT01728870
• Lead Sponsor: Prof. Arie Levine

Brief Summary

The purpose of this study is to assess the efficacy and tolerability of a novel dietary intervention for early CD based on partial enteral nutrition, and to compare it to the gold standard but difficult to implement dietary intervention- Exclusive enteral nutrition with Modulen .

Detailed Description

Background: Crohn's disease is clearly on the rise in countries exposed to industrialization and western diet. Several factors may implicate diet in the pathogenesis of CD or in disease activity. The strongest argument for an effect of diet is the effect of exclusive enteral nutrition (EEN) on disease activity in CD. 40-80% of children , fed an exclusive liquid diet, irrespective of which diet, will enter complete remission, often with normalization of inflammatory markers. The effect of formula has been shown to be independent of fat or protein composition in pediatric studies, but to be dependent on exclusion of normal diet.Thus, rather than the composition of EEN being associated with remission of disease it may be the exclusion of certain components of the Western diet may be responsible for improvement.

Methods:This is a prospective randomized controlled trial, in patients with a recent diagnosis of CD (up to two years),aged 4-18, comparing two arms over 12 weeks of therapy.

Group 1:will receive 50% of their dietary needs from a polymeric formula ( Modulen, Nestle) and a limited whole food diet for 6 weeks/ Group 2: will receive EEN with Modulen for 6 weeks. At the end of 6 weeks, all patients entering remission (irrespective of randomization) will enter the second 6 week phase, continuing 25 % of calories as Modulen in both groups. Patients in remission from group 2 will continue to consume 25% of calories as Modulen and be allowed free diet , patients in Group 1 will continue 25% of calories from Modulen but continue restricted diet.

Patients will be seen at onset (week 0), weeks 3 and 6, 12 and 24 weeks.

We hypothesize that by withdrawing the offending dietary agents we can achieve an equal remission rate with improved tolerability. This study will evaluate response, remission and tolerability in both groups, as well as the effects of nutrition on bone health.

Study Timeline

• Study First Submitted: 2012-11-13
• Study First Submitted QC: 2012-11-19
• Study First Posted: 2012-11-20
• Study Start: 2013-01
• Status Verified: 2018-07
• Primary Completion: 2018-07
• Study Completion: 2018-07
• Last Update Submitted: 2018-07-03
• Last Update Posted: 2018-07-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 74

Inclusion Criteria

1. Children 4-18 years of age.
2. Patients with a diagnosis of CD-duration of disease up to 36 months
3. Have macroscopic small bowel involvement, or isolated large bowel disease confined to the right or transverse colon
4. Patients with a pediatric activity index -PCDAI ≥ 10
5. Patients will not be excluded if they have received 5ASA or an immunomodulator for >8 weeks and the dose is stable , or if they start a thiopurine concurrently , as thiopurines are not considered sufficient to induce remission in active disease before 8 weeks as an isolated therapy.
6. Informed Consent

Exclusion Criteria

1. Patients with no disease activity ( PCDAI <10) or severe disease ( PCDAI ≥ 40).
2. Patients who have received corticosteroids of any kind in the previous 4 weeks.
3. Patients who have started an immunomodulator in the previous 8 weeks
4. Any current biological treatment
5. Isolated Large bowel disease ( L2) involving the recto-sigmoid or descending colon
6. Patients with penetrating disease (abscess or fistula)
7. Active Perianal disease
8. Fixed stricture or small bowel obstruction
9. Normal CRP and ESR
10. Active joint disease.
11. Patients who have undergone an intestinal resection.
12. Sclerosing Cholangitis
13. Pregnancy

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Unique Diet+Partial Enteral Nutrition	Unique Diet+Partial Enteral Nutrition	Unique Diet+Partial Enteral Nutrition (PEN): This group will receive as follows: Weeks 1-6: 50% of dietary needs from PEN (Modulen, Nestle) and 50% from a limited whole food diet. Weeks 7-12: 25% of dietary needs from PEN (Modulen, Nestle) and 75% from a limited whole food diet.
Exclusive Enteral Nutrition (Modulen)	Exclusive Enteral Nutrition (Modulen)	Exclusive Enteral Nutrition(EEN): This group will receive as follows: Weeks 1-6: EEN(100% of dietary needs from Modulen) Weeks 7-12: 25% of dietary needs from Modulen and 75% from a free diet.

Primary Outcome Measures

Name	Time	Method
patient's adherence with the diet assessed by cessation of therapy because of patients refusal to continue and by a MARS questionnaire	6 weeks

Secondary Outcome Measures

Name	Time	Method
Response, defined as a drop in PCDAI of 12.5 points or remission, on an intention to treat analysis.	6 weeks
Remission at week 6 and week 12 (defined as PCDAI≤10, or less than 7.5 without height component),	6 weeks and 12 weeks
Bone health	at the 3, and 6 month visits	change in serum bone biomarkers from baseline and their correlation with DEXA (optional)
CRP at week 12	12 weeks
Physician assessment of compliance	6 weeks

Trial Locations

Locations (3)

The E. Wolfson.Medical Center; 🇮🇱 Holon, Israel

University of Alberta; 🇨🇦 Edmonton, Alberta, Canada

IWK Health Centre; 🇨🇦 Halifax, Nova Scotia, Canada