Evaluation of Safety and Efficacy of Lumason/SonoVue in Subjects Undergoing Pharmacologic Stress BR1-141
Status:
Completed
Trial end date:
2018-02-25
Target enrollment:
Participant gender:
Summary
The purpose of this study was to assess the safety and efficacy of Lumason-enhanced
dobutamine stress echo (CE-DSE) in subjects having a suboptimal left ventricular endocardial
border delineation (LV EBD) at rest and who were scheduled for coronary angiography.