Study to Assess Limited Magnetic Resonance Imaging in the Surveillance of Crohn's Disease

Overview

About this study

The purpose of this study is to compare a limited magnetic resonance enterography (MREN) to routine MREN in order to determine non-inferiority, missed findings, patient tolerance and impact on patient management.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

Known Crohn’s disease.
Undergoing a routine clinical MR Enterography for routine surveillance or acute flare.

Exclusion Criteria:

Unable or unwilling to sign consent.
Contraindication to MR.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location	Status	Contact
Rochester, Minn. Mayo Clinic principal investigator Jeff Fidler, M.D.	Open for enrollment	Contact information: Brenda Becker CCRP (507) 266-0111 Becker.Brenda1@mayo.edu

Mayo Clinic Location

Status

Contact

Rochester, Minn.

Mayo Clinic principal investigator

Jeff Fidler, M.D.

Open for enrollment

Contact information:

Brenda Becker CCRP

(507) 266-0111

Becker.Brenda1@mayo.edu

More information

Publications

Publications are currently not available

Clinical Trials