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Safety and Efficacy of the Percutaneous Intervention Performed With Devices of a Single-brand — Tsunami  

Coronary Heart Disease Clinical Trial

Official title:
Safety and Efficacy of the Percutaneous Intervention Performed With Devices of a Single-brand

Clinical Trial Summary

The freedom of choice in medicine is based on the physician's ability to treat their patients with the best available therapy. The armamentarium for percutaneous intervention is frequently determined on the basis of subjective criteria and the experience of the interventional cardiologist. The evaluation of devices used in coronary intervention, especially angiography and its clinical outcomes, has rarely been investigated; the exceptions are studies on stents. Therefore, the freedom of choice for the interventional cardiologist has been challenged, especially because of cost restrictions. This way this study aims to assess the safety and efficacy of a device of a single brand in performing percutaneous transluminal coronary angioplasty (guide catheters, guidewires, balloons, and stents) in selected patients.

Clinical Trial Description

n/a

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01632501
Study type Interventional
Source Hospital Sao Lucas da PUCRS
Contact
Status Completed
Phase N/A
Start date January 2011
View Details
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