Evaluation of the Effectiveness of Kits Promonitor-IFX/ADL and Promonitor-Anti-IFX/ADL in Patients With IBD

CompletedOBSERVATIONAL
Enrollment

209

Participants

Timeline

Start Date

January 16, 2017

Primary Completion Date

October 3, 2019

Study Completion Date

May 8, 2023

Conditions
Crohn Disease and Ulcerative Colitis
Interventions
DEVICE

Use of the test for treatment optimization

Intervention cohort, where the clinician will have information on the test results to support decision making on treatment optimization. The randomization process will be by blocks and weighted to the ADL/IFX ratio of use of these treatments in the usual clinical practice of the participating hospitals, to guarantee a homogeneous distribution of the treatments in the groups at the beginning/end of the follow-up.

Trial Locations (1)

48013

Basurto University Hospital, Bilbao

All Listed Sponsors
collaborator

PROGENIKA BIOPHARMA, A GRIFOLS Company

UNKNOWN

lead

Hospital de Basurto

OTHER

NCT06666569 - Evaluation of the Effectiveness of Kits Promonitor-IFX/ADL and Promonitor-Anti-IFX/ADL in Patients With IBD | Biotech Hunter | Biotech Hunter