Crohn's Disease Clinical Trial
Official title:
A Randomized, Controlled Study of Soluble Dietary Fiber on Bacterial Translocation in Adults Patients With Crohn's Disease
Verified date | April 2018 |
Source | Jinling Hospital, China |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to evaluate the effect of soluble dietary fiber on bacterial translocation and mucosal immunology in patients with Crohn's disease.
Status | Terminated |
Enrollment | 3 |
Est. completion date | June 2017 |
Est. primary completion date | May 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 17 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Patients aged >=17 years with diagnosis of CD for at least 3 months defined by histology or radiology - ileocolonic non-penetrating disease - Moderate active CD with CDAI 250-450 - CRP level over normal range - Stable CD therapy with a total steroid dose not exceeding 10mg prednisolone or equivalent for 4 weeks Exclusion Criteria: - Infection with enteric pathogen - Usage of probiotics, antibiotics, or prebiotics within the last month - Change in dose of oral steroids or 5-ASA within the last 4 weeks or AZA or MTX in the last 3 months - Dose of steroids exceeds 10 mg prednisolone per day or equivalent - Infusion of IFX or any alternative biological therapy within the last 3 months - Use of rectal 5-ASA or steroids within the last 2 weeks. - Imminent need for surgery or presence of severe disease (CDAI >450) - Pregnancy or lactation - Short bowel syndrome or subtotal/total colectomy - Pure anal disease and previous proctocolectomy - Significant hepatic, renal, endocrine, respiratory, neurological or cardiovascular disease as determined by the principal investigator - History of cancer with a disease-free state of less than two years - Patients with penetrating disease or small bowel lesion only. |
Country | Name | City | State |
---|---|---|---|
China | Department of Generay Surgery, Jinling hosptal, Medical School of Nanjing University | Nanjing | Jiangsu |
Lead Sponsor | Collaborator |
---|---|
Jinling Hospital, China |
China,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | bacteria translocation in MLN, mesenteric fat and peripheral blood | Bacterial translocation to mesenteric lymph nodes (MLN),mesenteric fat and peripheral blood during laparotomy before surgical mobilization, as determined by DGGE. | 4 weeks after treatment | |
Secondary | change of fecal bacteriology | fecal microbiology before and 4 weeks after pectin treatment, as determined by DGGE | baseline, week 4 | |
Secondary | change of fecal SCFA | fecal short chain fatty acid (SCFA) levels before and 4 weeks after treatment, as determined by HPLC. | baseline, week 4 | |
Secondary | clinical response | the percentage of patients achieving a clinical response (fall in CDAI of >=70 points) at week 4. | up to 4 weeks after treatment | |
Secondary | change of mucosal Treg numbers | mucosal Treg(FoxP3+CD4+)cell number before and after treatment,as determined by immunofluorescence | baseline, week 4 | |
Secondary | adverse events | gastrointestinal symptoms(borborygmi,flatulence,abdominal pain,diarrhea etc) | up to 4 weeks after treatment |
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