Gastroduodenal ulcer and after ESD artificial ulcer
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients of gastroduodenal ulcer or after ESD artifical ulcer
Exclusion criteria
Exclusion criteria: 1. Patients continuously using PPI or Vonoprazan 2. Women with pregnancy or possible pregnancy 3. Patients with severe renal failure and heart failure 4. Patient who is considered to be inappropriate for entry into the trial by the investigator 5. Medical doctors decided the patients are inappropriate 6. Patient who has allergy to drugs or foods used in this research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the change of Gut microbiota caused by using Vonoprazan and kestose or placebo for 8 weeks | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Ovserbation of the change of ulcer healing caused by kestose 2. Changes of short-chain fatty acid (Butyric acid,Acetic acid,Propionic acid etc.) 3. Changes of pathologic and metabolic marker (T.Cho, LDL-Cho, HDL-Cho, TG, FFA, ferritin,HbA1c,CRP,TP,ALB etc.) 4. Correlation of gut microbiota and bowel habits 5. Changes of body weight and BMI 6. Metabolome,bile acid and protein analysis of metabolite in feces 7. Correlation between expiratory noble gases,gut microbiota and ulcer healing | — |
Countries
Japan
Contacts
Nagoya University Hospital Department of Gastroenterology and Hepatology