Ulcerative colitis
Conditions
Interventions
arm A Kestose(10g) every day 8 weeksar
arm B Maltose(5g) every day 8 weeks
Sponsors
Honda Takashi
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with active ulcerative colitis (Lichtiger CAI>3)
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 ulcerative colitis | — |
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 ulcerative colitis 10.Correlation between usefulness of kestose and disease prognosis in the patients with ulcerative colitis | — |
Contacts
Public ContactSyuuji Ikegami
Nagoya university
Outcome results
None listed