Post-Market CorPath Registry on the CorPath 200 System in Percutaneous Coronary Interventions

Completed

Conditions studied: Coronary Artery Disease, Coronary Disease, Myocardial Ischemia, Heart Diseases, Cardiovascular Diseases, Arteriosclerosis, Arterial Occlusive Diseases, Vascular Diseases

In brief

To collect data on the routine patterns of use, safety and effectiveness, including the clinical and technical performance of the CorPath 200 System, in the delivery and manipulation of coronary guidewires and stent/balloon catheters during PCI procedures.

Key facts

Study ID
NCT01917682
Run by
Siemens Healthineers Endovascular Robotics, Inc.
People needed
754
Starts
2013-08-01
Expected to finish
2016-12-01
Last updated by the study team
2020-12-22

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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