Crohn Disease Clinical Trial
— CDOfficial title:
Impact of Anti-Inflammatory Whole-Food Diet in Crohn's Disease and Predicting Response to Therapy
NCT number | NCT04431700 |
Other study ID # | 20-001120 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | October 5, 2020 |
Est. completion date | May 1, 2025 |
Patients with inflammatory bowel disease (IBD) often have narrowed microbial diversity and altered composition and function of the gut microbiome. We anticipate the anti-inflammatory diet, when compared with the usual diet, to produce favorable changes in these multi-omics profiles. These findings will provide insight into the interactions between diet and host biology, while providing clues on the mechanisms of diet therapy's effect and CD pathogenesis.
Status | Recruiting |
Enrollment | 116 |
Est. completion date | May 1, 2025 |
Est. primary completion date | January 31, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion Criteria: - Age of 18 to 75 years old - History of Crohn's Disease (CD) with mild to moderate symptoms and prior biopsy proof Exclusion Criteria: 1. History or current diagnosis of any of the following: - Stroke or Arrhythmia - Seizures - Liver Disease - Untreated hypertension (High Blood Pressure) - Active malignancy - Bleeding disorders - Heart Disease - Lung disease - Previous Heart surgery - Previous Gastrointestinal Surgery - Kidney Disease - Chronic Diarrhea - End enterostomy - Bulimia - Anorexia - Laxative Abuse - Endocrine Disorder - Current history of smoking tobacco - Urgent need for abdominal sugery - Severe Malnutrition - Active alcohol or non-cannabinoid substance abuse 2. Recent hospitalization within the last 30 days 3. Currently pregnant of lactating. 4. Current use probiotics or dietary supplements that would not be willing to discontinue for the length of the study. 5. Concerns for non-compliance 6. If currently on immunosuppressants, immunomodulators, cotticosteroids, and/or 5-aminosalicylates, no changes in doses will be permitted during the trial except for tapering of corticosteroids. |
Country | Name | City | State |
---|---|---|---|
United States | UCLA Center for Human Nutrition, 1000 Veteran Ave. | Los Angeles | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Los Angeles |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Efficacy of the anti-inflammatory whole food diet for the induction of remission in Crohn's Disease | The patients' clinical response, defined by the Harvey-Bradshaw Index (HBI) (5 through 16 points) for clinical symptom improvement and/or remission. | 8 weeks |
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