The patients with unexplained abdominal symptoms
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Age: 20 years old or older Gender: any gender Subjects: Patients with unexplained abdominal symptoms and patients without abdominal symptoms
Exclusion criteria
Exclusion criteria: Patients who cannot give their consent to participate in this study. Patients who are unable to collect specimens due to defecation problems.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Total bile acid concentration in stool | — |
Secondary
| Measure | Time frame |
|---|---|
| Biochemical markers (TP, Alb, AST, ALT, GTP, BUN, Cre, UA, CRP, TG, T-cho, LDL-C, endotoxin, various antibodies, various vitamins, etc.) -Hematological examination (WBC, Hb, Plt, PT, APTT, erythrocyte sedimentation rate, etc.) -Blood metabolome analysis -Hydrogen breath test Lactulose-mannitol test Imaging findings (abdominal x-ray with Schitzmark, abdominal ultrasound, abdominal CT, Cine-MRI, endoscopic findings, etc.) -Pathological findings -Stool metabolome analysis, organic acid analysis -Bile metabolome analysis -Urinary metabolome analysis -Clinical findings, history, complications, and medication history -Questionnaire/Questionnaire -Fecal microbiota analysis | — |
Countries
Japan
Contacts
International university health and welfare Narita hospital Palliative medicine and Gastroenterology