Overview

Long Term Prophylactic Therapy of Congenital Long QT Syndrome Type III (LQT3) With Ranolazine

Status:
Unknown status
Trial end date:
2017-11-01
Target enrollment:
0
Participant gender:
All
Summary
The purpose of this study is to determine whether ranolazine will reduce the risk of arrhythmic events in patients with long QT syndrome type 3.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Tel-Aviv Sourasky Medical Center
Treatments:
Ranolazine
Criteria
Inclusion Criteria:

- Long QT patients with genetic confirmation of carrier-status for the D1790G mutation
in the SCN5A gene

- Corrected QT interval > 460 msec

Exclusion Criteria:

- Need for therapy with medications that are potent or moderately potent CYP3A
inhibitors (such as ketoconazole, diltiazem, verapamil, macrolide antibiotics or HIV
protease inhibitors)