Ulcerative colitis
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: (1) UC patients who plan to receive biologics (2) Persons who have obtained written consent to participate in the research (3) Gender does not matter (4) Persons who are 16 years of age or older at the time of obtaining consent
Exclusion criteria
Exclusion criteria: (1) Persons who did not obtain consent after the explanation (2) Those who cannot get an understanding by explaining it verbally (3) Persons who have already been administered biopharmacy at the time of obtaining consent (4) Partial Mayo score 2 points or less
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary outcome of this study is proportion of patients with primary non-response to biologics stratified by PR3-ANCA and MPO-ANCA positivity. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary outcome of this study is proportion of patients with loss of response to biologics stratified by PR3-ANCA and MPO-ANCA positivity. | — |
Countries
Japan
Contacts
Ofuna Chuo Hospital Center for Gastroenterology and Inflammatory Bowel Disease