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Assessment of CXC chemokine receptor type 4 (CXCR4) expression as a predictive marker on the effect of leukocytapheresis for ulcerative colitis

Assessment of CXC chemokine receptor type 4 (CXCR4) expression as a predictive marker on the effect of leukocytapheresis for ulcerative colitis - Assessment of CXC chemokine receptor type 4 (CXCR4) expression as a predictive marker on the effect of leukocytapheresis for ulcerative colitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005718
Enrollment
20
Registered
2011-06-06
Start date
2011-07-01
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

Patients treated with leukocytapheresis (more than once per week, total 10 sessions) therapy have a regular blood test

Sponsors

Kyoto University Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with moderate, severe or intractable ulcerative colitis 2) Patients with ulcerative colitis of left side colitis or pancolitis type 3) Patients whom immunomodulator doses are not changed for two months 4) Patients that steroid doses are not increased in quantity for one week

Exclusion criteria

Exclusion criteria: 1) Patients with proctitis 2) Patients with either white blood cell count of less than 3,000/mm3, or hemoglobin level of less than 10g/dL, or platelet count of less than 100,000/mm3 3) Patients with fulminating active ulcerative colitis (massive bleeding, perforation, toxic megacolon) 4) Patients with serious infection or cardiovascular disease or liver disease or kidney disease or respiratory disease or metabolic disease neurologic disease 5) Patients with hypotension (less than maximal blood pressure 80mmHg) 6) Patients with allergic anamnesis or experience or the fear of allergic hypersensitivity reaction 7) Patients having received inhibitor of angiotensin converting enzyme 8) Patients who are pregnant or have the possibility of pregnancy 9) Patients who are younger than 12 years old or low weight 10) Patients determined to be inappropriate for this study by the investigators

Design outcomes

Primary

MeasureTime frame
CXCR4 expression on CD4 positive T cell in peripheral blood

Countries

Japan

Contacts

Public ContactMinoru Matsuura

Kyoto University Hospital Department of Gastroenterology and Hepatology

minomats@kuhp.kyoto-u.ac.jp075-751-4319

Outcome results

None listed

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