Ultrasound Evaluation of Crohn's Disease

PHASE4TerminatedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

June 16, 2017

Primary Completion Date

October 12, 2021

Study Completion Date

October 12, 2021

Conditions
Crohn Disease
Interventions
DRUG

Sulfur Hexafluoride

Subjects will receive ultrasound (US) imaging of the terminal ileum without and with sulfur hexafluoride contrast at baseline, 4 week and 6 months. Subjects will receive one to two milliliters of the contrast agent.

DEVICE

Ultrasound Elastography

Subjects will receive US Imaging with the GE Logiq E9 Ultrasound Scanner at baseline, 4 week and 6 months without and with contrast.

DEVICE

Ultrasound Vascularity

Subjects will receive US Imaging with the Verasonics Ultrasound Scanner at baseline, 4 week and 6 months without and with contrast.

DEVICE

Magnetic Resonance Enterography (MRE)

Subjects will receive MRE imaging at baseline and 6 months as part of regular clinical care.

Trial Locations (1)

55902

Mayo Clinic, Rochester

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Mayo Clinic

OTHER