NIPH Clinical Trials Search

JAPANESE
国立保健医療科学院
UMIN ID: UMIN000054083

Registered date:07/06/2024

Investigation of preference, clinical efficacy and trough concentration of vedolizumab by patient-oriented switching to intravenous (IV) or subcutaneous (SC) injection in patients with ulcerative colitis

Basic Information

Recruitment status Recruiting
Health condition(s) or Problem(s) studiedulcerative colitis
Date of first enrollment2024/06/07
Target sample size50
Countries of recruitmentJapan
Study typeObservational
Intervention(s)

Outcome(s)

Primary OutcomeSelectivity of intraveous or subctaneous injection of vedolizumab
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum18years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1. Patients who has allergy to vedolizumab 2. Patients who determined to be inappropriate for this study by physician

Related Information

Contact

public contact
Name Shingo Kato
Address 1981, Kamoda, Kawagoe City, Saitama, Japan Japan 3508550
Telephone 0492283564
E-mail skato@saitama-med.ac.jp
Affiliation Saitama Medical Center, Saitama Medical University Department of Gastroenterology and Hepatology
scientific contact
Name Shingo Kato
Address 1981, Kamoda, Kawagoe City, Saitama, Japan Japan
Telephone 0492283564
E-mail skato@saitama-med.ac.jp
Affiliation Saitama Medical Center, Saitama Medical University Department of Gastroenterology and Hepatology