Ulcerative Colitis
Conditions
Interventions
None listed
Sponsors
Showa University Koto Toyosu Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients who have received complete information about the study and are willing to provide written informed consent.
Exclusion criteria
Exclusion criteria: 1:Inability or unwillingness of patients to give written informed consent 2:Judged unsuitable for this study by the physician
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1:Try to identify molecules that could correlate with endoscopic findings(UC-EIS) before treatment and at 10 weeks on therapy. 2:To test whether a novel biomarker could be used to predict mucosal healing at 1 year after treatment initiation. | — |
Secondary
| Measure | Time frame |
|---|---|
| 1:To evaluate the correlation between the new biomarker(s) and UCDAI score at 1,4,10 weeks and 1year after treatment. 2:To evaluate the correlation between the new biomarker(s) and Matts grade at 10 weeks after treatment. | — |
Countries
Japan
Contacts
Public ContactAkiko Toshimori
Showa University Koto Toyosu Hospital Digestive Disease Center
Outcome results
None listed