The purpose of this investigation is to compare subjects at high risk for silent myocardial ischemia in the placebo group to subjects at high risk for silent myocardial ischemia in the ranolazine group to determine if ranolazine can be used as a treatment to decrease silent myocardial ischemia (SMI). Subjects at high risk for silent myocardial ischemia are defined in this protocol as diabetics with stable ischemic heart disease. This study will look at the impact ranolazine treatment has on biomarkers that have been shown to be highly associated with increased risk of morbidity and mortality in relation to SMI. If the hypothesis is correct, further studies can be conducted to determine if treatment with ranolazine has impact on long-term outcomes such as hospitalizations, myocardial infarction, congestive heart failure or sudden cardiac death.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
TRIPLE
24 weeks of the assigned medication
Placebo for 24 weeks
hs cTnT
Does ranolazine decrease hs cTnT in subjects at high risk for silent myocardial ischemia?
Time frame: 24 weeks
NT-pro-BNP
Does ranolazine decrease NT-pro-BNP in subjects at high risk for silent myocardial ischemia?
Time frame: 24 weeks
hsCRP
Determine the degree of decrease of hs CRP in subjects in the ranolazine group.
Time frame: 24 weeks
prevalence of hs cTnT > 99th percentile
Determine the prevalence of hs cTnT greater than the 99th percentile (0.014 ng/mL) in asymptomatic diabetic subjects with stable ischemic heart disease.
Time frame: 24 weeks
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