Dietary Treatment of Crohn's Disease

Rush

Status and phase: Completed; Phase 2; Phase 1

Conditions: Inflammatory Bowel Disease; Crohn's Disease

Treatments: Dietary Supplement: Diet; Drug: Active fructo-oligosaccharide; Drug: Placebo fructo-oligosaccharide

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00343642

R21AT001628-01A2 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

Our objective is to determine whether a specific dietary intervention or a fructooligosaccharide (FOS) supplement has anti-oxidant or prebiotic effects and whether it is beneficial in the treatment of Crohn's Disease (CD.

Full description

Several epidemiological studies and therapeutic observations in the complementary and alternative medicine (CAM) literature suggest that diet is key to development of CD and its treatment. The investigators took advantage of these CAM recommendations and designed dietary interventions. Our preliminary open label studies in IBD patients showed that our interventions are acceptable and well-tolerated and result in improvement, reducing symptoms and/or the degree of inflammation. The investigators are now seeking to validate this finding and determine the mechanisms underlying the effects of dietary manipulation-such as potential effects on colonic bacterial microflora. In another pilot study using 16s rDNA bacterial fingerprinting, the investigators demonstrated that the intestinal microflora of patients with CD differ significantly from healthy individuals. Whether the investigators can normalize/change the microflora of CD patients with dietary therapies, however, remains to be determined. Accordingly, the investigators designed a double blind placebo controlled study to test the hypotheses that: (1) dietary manipulation with either diet or a FOS supplement is an effective CAM therapy that prevents CD relapse (leads to maintenance of remission) and (2) such dietary manipulation can normalize the microflora of CD patients and decrease mucosal oxidative damage.

90 participants are expected to undergo the trial and have a 2:1 chance of receiving active therapy. The trial is seeking to enroll participants with inactive CD who have been medically induced into remission within 9 months of enrollment. Participants must be on their Crohn's medications at a stable dose for 3 months, which does not include steroids (e.g. Prednisone, Entocort) or antibiotics at the time of enrollment. Participants will be followed till relapse occurs or up to 52 weeks. Participants are asked to fill out a variety of questionnaires, keep a food and adverse event diary, and have a research, limited, unprepped flexible sigmoidoscopy for colonic tissue collection at the beginning and end of the study period.

Significance. This study could provide information to suggest diet or dietary supplement as a safe therapy for IBD and lay the groundwork for more definitive, randomized, controlled trials.

Enrollment: 73 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Documented ileocolonic or colonic CD based on classical history and classical endoscopic or surgical findings and histology compatible with CD;
2. Induction of remission with medical therapy within 9 months of the study;
3. Inactive CD for at least 2 weeks with CDAI score less than 150;
4. No change in IBD medication doses for 3 months;
5. No change in smoking habits a month prior to enrollment (because smoking may exacerbate CD) and acceptance of not-changing smoking habits during the term of the study).

Exclusion criteria

1. Patients with history of bowel obstruction and/or known strictures (as the high fiber content may precipitate obstruction);

2. Patients with extensive colonic or ileocolonic resection;

3. Patients with ileostomies or colostomies with diverted fecal stream;

4. Patients with isolated perianal/anorectal disease;

5. Patients with surgically induced remission;

6. Concomitant infection (e.g., C. difficile colitis);

7. Use of antibiotics within 4 weeks, or steroids, herbal remedies or diet therapies within 2 weeks of the onset of the trial or during the study;

8. Use of potential IBD exacerbators such as NSAIDs within 1 wk of the study;

9. Acute illness requiring immediate hospitalization for CD or other reasons;

10. Presence of symptomatic organic GI disease other than CD, hemorrhoids, hiatal hernia; GERD;

11. Pre-existent organ failure or severe comorbidities as these may change Gl flora:

    • Liver disease (cirrhosis or persistently abnormal AST or ALT that are 2X> normal);
    • Kidney disease (creatinine>2.0 mg/dL);
    • Uncontrolled psychiatric illness;
    • Clinically important lung disease or heart failure;
    • HIV disease;
    • Alcoholism;
    • Transplant recipients;
    • Patients receiving other immunosuppressant medications for comorbidities (e.g. Enbrel for rheumatoid arthritis);

12. Presence of short bowel syndrome or severe malnutrition with ideal body weight less than or equal to 90% or predicted;

13. Estimated survival <1 year and Karnofsky performance status <50%;

14. Desire to become pregnant during study or current pregnancy or nursing;

15. Desire to change smoking-status during the study;

16. Daily use of anticoagulation and antiplatelet medications;

17. Complicated IBD with anticipation of imminent surgical intervention during the term of the study;

18. Inability to have a regular follow-up and comply with study requirements.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Single Group Assignment

Masking: Triple Blind

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73 participants in 3 patient groups, including a placebo group

Active Fructo-oligosaccharide

Experimental group

Description:

Subjects received an active fructo-oligosaccharide supplement and a diet following the 2005 Dietary Guidelines for Americans. The fructo-oligosaccharide supplement was administered orally in a powder form two teaspoons daily.

Treatment:

Drug: Active fructo-oligosaccharide

Placebo Fructo-oligosaccharide

Placebo Comparator group

Description:

Subjects received a placebo fructo-oligosaccharide supplement and a diet following the 2005 Dietary Guidelines for Americans.

Treatment:

Drug: Placebo fructo-oligosaccharide

Dietary Therapy

Active Comparator group

Description:

Subjects received a placebo fructo-oligosaccharide supplement and a restrictive anti-inflammatory diet developed by the research team.

Treatment:

Dietary Supplement: Diet