The EDICT Trial - Therapy for Inflammatory Bowel Disease Flares

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21+
SponsorWake Forest University Health Sciences

About this trial

Inflammatory bowel disease (IBD), including Crohn's disease (CD) and ulcerative colitis (UC), are chronic inflammatory conditions of the gastrointestinal tract that affect millions of people in the United States of America. Among patients with IBD, symptomatic flares are quite common; up to 40-50% of patients in some populations report having a flare at least once per month. For most patients with IBD flares, the typical outpatient treatment consists of corticosteroids and, in some instances, initiation of or switching between 5-aminosalicylic acid-acid preparations, immunomodulators, or biologics. These treatments, while often effective, can have harmful side effects, especially when used for long durations of time. Therefore, alternative treatments are highly sought after by both patients and providers.

Eligibility criteria

Qualifiers

adults with an established diagnosis of inflammatory bowel disease (ulcerative colitis or Crohn's disease) who are being treated in the outpatient setting for an Inflammatory bowel disease (IBD) flare, defined as a clinically significant increase in IBD symptoms (e.g., abdominal pain, nausea, vomiting, diarrhea, joint pain, fever, bleeding, unintended weight loss).

Disqualifiers

Patients requiring admission to the hospital for treatment of a flare

Patients with allergies to any ingredients in the mBIOTA Elemental Diet

Female patients who are pregnant

Patients with diabetes who are taking insulin as part of their treatment plan

Trial design

Treatments tested in this trial

  • elemental diet (ED)

Treatment groups

42 Participants
are divided into 2 treatment groups

Sponsors and collaborators