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
Sponsors and collaborators
Wake Forest University Health Sciences
Lead sponsor
mBIOTA
Collaborator