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Effect of Ranolazine on Echocardiographic Indices of Diastolic Dysfunction

The Effect of Ranolazine on Echocardiographic Indices of Diastolic Dysfunction

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00574756
Enrollment
14
Registered
2007-12-17
Start date
2007-12-31
Completion date
2010-03-31
Last updated
2019-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diastolic Heart Failure, Echocardiography, Ranolazine, Tissue Doppler Ultrasound

Brief summary

The purpose of this study is to evaluate the effects of ranolazine, an FDA-approved medication for the treatment of angina, on heart function by using echocardiography.

Interventions

DRUGranolazine

extended release 500 mg twice a day for two weeks

Sponsors

University of California, San Diego
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Moderate of severe diastolic dysfunction, E/Ea\>12 * Preserved systolic function * NYHA Class I-II

Exclusion criteria

* QTc \>450 msec at enrollment * Taking medications that prolong QT interval or are potent inhibitors of CYP3A * Significant coronary artery disease * Severe valvular disease * Hepatic disease * Severe kidney disease * Women of childbearing age * Prior serious ventricular arrhythmia

Design outcomes

Primary

MeasureTime frame
Change in E/Ea2 weeks

Secondary

MeasureTime frame
changes in mitral inflow parameters (E, A, IVRT, DT)2 weeks
Changes in tissue doppler parameters (Ea, Aa)2 weeks
Changes in pulmonary venous inflow (S, D, a reversal)2 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026