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A Post-Market Registry for the Evaluation of the CorPath 200 System Effectiveness in Percutaneous Coronary Interventions

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Trial Conditions
  • Coronary Artery Disease
  • Coronary Disease
  • Myocardial Ischemia
  • Heart Diseases
  • Cardiovascular Diseases
  • Arteriosclerosis
  • Arterial Occlusive Diseases
  • Vascular Diseases
What is the purpose of this trial?

The purpose of the study is to collect additional information on the safety and effectiveness of the CorPath 200 system now that it is cleared for use by physicians in the delivery and manipulation of coronary guidewires and balloons/stents during percutaneous coronary interventions. The study is designed to collect information from the routine use of the CorPath 200 system.

Date & Status

Not yet recruiting

Who can Participate?


18 and older



Inclusion Criteria:

1. Age >18 years.

2. Patients with coronary artery disease undergoing Percutaneous Coronary Intervention
(PCI) with the CorPath 200 system.

3. The subject or the legal representative has been informed of the nature of the study,
agrees to its provisions and has provided written informed consent.

Exclusion Criteria:

1. Concurrent enrollment in another device or drug study protocol that specifically
excludes concurrent enrollment or that prevents collection of data required in this
registry (concurrent participation in another registry is not an automatic exclusion
criterion for this study).

2. Failure/inability/unwillingness to provide informed consent.

Gender: Both
Steward Physician(s)
  • Giora Weisz, MD
  • Chris Cain
  • Tal Wenderow
Trial Interventions
  • CorPath-assisted Percutaneous Coronary Intervention
Physician Researcher

Investigator Name:

  • Giora Weisz, MD
  • Chris Cain
  • Tal Wenderow

Other Information

Sponsor: Corindus Inc.
Phase: N/A
Trial ID: NCT01917682
Volunteers:  Not Accepting Healthy Volunteers

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