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The study of ANCA for efficacy of biologics therapy in patients with ulcerative colitis

The study of anti-neutrophil cytoplasmic antibody(ANCA) for efficacy of biologics therapy in patients with ulcerative colitis - The study of ANCA for efficacy of biologics therapy in patients with ulcerative colitis

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000043883
Enrollment
200
Registered
2021-04-10
Start date
2021-04-08
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ulcerative colitis

Interventions

None listed

Sponsors

Center for Gastroenterology and Inflammatory Bowel Disease, Ofuna Chuo Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

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

MeasureTime 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

MeasureTime 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

Public Contactatsushi yoshida

Ofuna Chuo Hospital Center for Gastroenterology and Inflammatory Bowel Disease

atushi.y@kza.biglobe.ne.jp0467-45-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026