90
Participants
Start Date
July 3, 2019
Primary Completion Date
October 31, 2024
Study Completion Date
October 31, 2024
Gadavist 15Ml Solution for Injection
Group 2 (n=30) will receive the clinically approved gadobutrol (Gadavist, 0.1mmol/kg) as contrast agent. The contrast agents will be administered at a flow rate of 5.0 ml/s for both groups. In this study aim, all imaging protocols will comply with standard of care and only the perfusion data will be post-processed and analyzed.
Medical University of South Carolina, Charleston
Collaborators (1)
Guerbet
INDUSTRY
Medical University of South Carolina
OTHER