91
Participants
Start Date
July 31, 2012
Primary Completion Date
July 5, 2019
Study Completion Date
November 16, 2020
regadenoson infusion with contrast-enhanced ultrasound
Subjects who are not having a pain crisis receive a 24-hour infusion of regadenoson. Contrast-enhanced ultrasound will be performed four times during the 24 hour regadenoson infusion
contrast-enhanced ultrasound
Subjects who are not having a pain crisis will have contrast-enhanced ultrasound performed up to four times over a two-day period. Time points will resemble the time course used for the Regadenoson Arm, although no investigational drug will be given.
contrast-enhanced ultrasound
Contrast-enhanced ultrasound will be performed on adults with sickle cell anemia at baseline who are not having a pain crisis and performed again during a pain crisis
contrast-enhanced ultrasound
Contrast-enhanced ultrasound will be performed on healthy control subjects at baseline, on the first day of the study and 30 days later
contrast-enhanced ultrasound
Contrast-enhanced ultrasound will be performed on healthy volunteers (Technique Optimization Controls)
Medical College of Wisconsin, Milwaukee
The University of Illinois, Chicago
Medical College of Wisconsin
OTHER
La Jolla Institute for Allergy & Immunology
OTHER
University of Illinois at Chicago
OTHER
Oregon Health and Science University
OTHER
Dana-Farber Cancer Institute
OTHER
Versiti
OTHER