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Phase 2 N=26 Randomized Quadruple-blind Treatment

Microvascular Assessment of Ranolazine in Non-Obstructive Atherosclerosis (MARINA)

Microvascular Angina

Enrolled (actual)
26
Serious AEs
0.0%
Results posted
May 2019
Primary outcome: Primary: Change in Seattle Angina Questionnaire Score Regarding Angina Frequency — 0.70; 0.27 score on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Ranolazine (Drug); Placebo (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Emory University
Primary completion
Mar 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Change in Seattle Angina Questionnaire Score Regarding Angina Frequency
0.70; 0.27
SECONDARY
Change in Seattle Angina Questionnaire Score Regarding Physical Limitation
-0.09; 0.27
SECONDARY
Change in Seattle Angina Questionnaire Score Regarding Angina Stability
0.00; 0.50
SECONDARY
Change in Seattle Angina Questionnaire Score Regarding Treatment Satisfaction
1.17; 0.28
SECONDARY
Change in Seattle Angina Questionnaire Score Regarding Disease Perception
0.89; 1.00
SECONDARY
Change in Peak Rate of Oxygen Consumption (VO2 Max)
-0.03; 0.06
SECONDARY
Change in Time to Angina
SECONDARY
Change in Metabolic Equivalents of Task (METs) at Peak
0.00; 4.42
SECONDARY
Change in Coronary Flow Reserve (CFR)
0.38; 0.09
SECONDARY
Change in Hyperemic Microcirculatory Resistance (HMR)
0.14; -0.04
SECONDARY
Percent Change in Coronary Blood Flow

Summary

The purpose of this study is to look at the effects of the drug Ranolazine compared to Placebo on symptoms of chest pain or chest tightness (known as angina), exercise endurance and ability, and changes in blood flow to the very small arteries of the heart (known as coronary microvascular function) in patients who do not have significant blockages in their major heart arteries. Ranolazine is a drug that is already approved by the FDA for angina, but it may be particularly effective in people with disease in their tiny heart vessels (known as coronary microvascular disease). This trial aims to enroll 50 patients with angina who undergo baseline bicycle exercise testing with monitoring of the heart's electrical activity and oxygen consumption (known as cardiopulmonary exercise test) and coronary angiogram (taking pictures of the heart arteries through small hollow tubes placed through the wrist or groin). If severe blockages in the main arteries are not found then testing for coronary microvascular function will be performed. Subsequently, participants will then be randomized 50/50 to either Ranolazine or Placebo. After taking the study drug for 12 weeks, they will then repeat the cardiopulmonary exercise test and the coronary angiogram with testing for microvascular function.

Eligibility Criteria

Inclusion Criteria

  • History of typical angina or effort-induced anginal symptoms and are currently experiencing angina at least once per week
  • Abnormal stress ECG, exercise stress imaging, or pharmacological stress imaging
  • Non-obstructive coronary artery disease as defined by lesion stenosis ≤ 50% in any artery as visualized by diagnostic angiography

Exclusion Criteria

  • Inability to provide informed consent
  • Active Myocardial Infarction
  • History of coronary artery bypass grafting
  • Diagnosis of other specific cardiac disease such as severe valvular heart disease, cardiomyopathy, or variant angina
  • Left Ventricular Ejection Fraction (LVEF) < 30%
  • Known renal insufficiency (CrCl < 30 mL/min) or on dialysis
  • Contraindications to the use of Ranolazine
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02147067). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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