Cardiovascular Systems Presents Results from Pivotal Coronary Trial at ACC
ORBIT II trial met its primary endpoints treating one of the most challenging patient populations:
100 percent of patients had severe coronary calcification—a patient subset never before studied
At 30 days, patient outcomes exceeded the study’s primary safety and efficacy endpoint targets by a significant margin
30-day freedom from MACE rate of 89.8 percent
Procedural success of 89.1 percent (including in-hospital MACE)
Cardiovascular Systems, Inc. (CSI) (CSII), presented pivotal 30-day data from its ORBIT II study of severely calcified coronary lesions at the 2013 American College of Cardiology (ACC) conference in San Francisco.
- Published: 11 March 2013
- Written by Editor