Trial Details

COMPLETED
Basic Information
Clinical ID c1655
Identifier NCT06666569
Trial Title Evaluation of the Effectiveness of Kits Promonitor-IFX/ADL and Promonitor-Anti-IFX/ADL in Patients With IBD
Trial URL Visit Original Page
Study Information
Study Results

NO

Conditions Crohn Disease and Ulcerative Colitis
Interventions DEVICE: Use of the test for treatment optimization
Participant Information
Sponsor Hospital de Basurto
City Bilbao
Country/Region Spain
Enrollment Criteria
Sex Requirement ALL
Age Requirement ADULT, OLDER_ADULT
Study Design
Study Type OBSERVATIONAL
Phase -
Time Information
Start Date 2017-01-16
Primary Completion Date 2019-10-03
Completion Date 2023-05-08