The ROB-OSTIAL Study
Coronary Artery Disease
About this trial
This is an interventional treatment trial for Coronary Artery Disease focused on measuring Ostial Lesion, Robotic-assisted PCI, PCI
Eligibility Criteria
Inclusion Criteria: Male or nonpregnant female aged ≥18 years Coronary OSTIAL lesion suitable for percutaneous coronary intervention (PCI) The subject has been informed of the nature of the study, agrees to its provisions and has provided written informed consent. Exclusion Criteria: Cardiogenic shock or hemodynamic instability requiring support. ST-elevation myocardial infarction. Ongoing acute renal failure. In the opinion of the investigator, the subject is deemed unsuitable for robotic PCI due to clinical status and/or anatomic characteristics More than one lesion to be treated Ostial left main disease
Sites / Locations
- Maria Cecilia Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Robotic-assisted PCI with Corpath GRX® System
Standard PCI
Percutaneous coronary intervention (PCI) using the Corpath GRX System.
Percutaneous coronary intervention (PCI) using manual techniques. This arm will be completed without robotic assistance.