Inflammatory Bowel Disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients diagnosed as Inflammatory Bowel Disease(ulcerative colitis,crohn disease)
Exclusion criteria
Exclusion criteria: 1.Women with pregnancy or possible pregnancy 2.Patients with severe renal failure and heart failure 3.Patient who is considered to be inappropriate for entry into the trial by the investigator 4.Medical doctors decided the patients are inappropriate.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Improvement of clinical condition in patients with Inflammatory Bowel Disease | — |
Secondary
| Measure | Time frame |
|---|---|
| 1.Changes of short-chain fatty acid (Butyric acid,Acetic acid,Propionic acid etc.) 2.changes of endoscopic score 3.changes of concentration of carprotectin in feces 4.Changes of pathologic and metabolic marker (T.Cho, LDL-Cho, HDL-Cho, TG, FFA, ferritin,HbA1c,CRP,TP,ALB etc.) 5.Correlation of gut microbiota and therapeutic effect 6.Changes of body weight and BMI 7.Metabolome and protein analysis of metabolite in feces 8.Changes of bile acid 9.Correlation between expiratory noble gases, gut microbiota and NAFLD/NASH 10.Correlation between usefulness of kestose and disease prognosis in the patients with Inflammatory Bowel Disease | — |
Countries
Japan
Contacts
Nagoya University Hospital Department of Gastroenterology and Hepatology