Last updated on July 2019

REDUCER-I: An Observational Study of the Neovasc Reducer System

Brief description of study

The purpose of this study is to collect long term data of the Neovasc Reducer System in subjects with refractory angina pectoris.

Detailed Study Description

This study is a multicenter, multi-country three-arm prospective and retrospective investigation in up to 400 subjects conducted at a maximum of 40 investigational centers. Arm 1 will include eligible prospective subjects. Arm 2 will include subjects who were previously enrolled and treated with the Reducer during the COSIRA (Coronary Sinus Reducer for Treatment of Refractory Angina) study. Arm 3 will include subjects who received a Reducer under CE Mark (unrelated to the COSIRA study).

Clinical Study Identifier: NCT02710435

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