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Effect of Ranolazine on Activity Level in Patients With Angina After FFR Based Deferred Intervention (REPTAR) — REPTAR  

Angina Clinical Trial

Official title:
Effect of Ranolazine on Activity Level in Patients With Angina After FFR Based Deferred Intervention

Clinical Trial Summary

The post-marketing study is designed to evaluate the activity level and exercise tolerance of patients with deferred percutaneous intervention due to FFR (fractional flow reserve) greater or equal to 0.81 and treatment with Ranolazine versus placebo.

Clinical Trial Description

Ranolazine was approved as Ranexa in the United States on January 31, 2006 for the treatment of chronic angina. This post-marketing study is a single-center, double-blind, prospective, randomized, parallel-group evaluation of patients randomized 1:1 between Ranolazine and placebo. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03044964
Study type Interventional
Source Stern Cardiovascular Foundation, Inc.
Contact Amit Malhotra, MD
Phone 901-271-5468
Email amit.malhotra@sterncardio.com
Status Recruiting
Phase Phase 4
Start date January 10, 2017
Completion date October 2017
View Details
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