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Study identifier: NCT06600178 Synced from ClinicalTrials.gov · July 29, 2026
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Study Targeting Myocardial Perfusion and Symptom Relief in Women With SGLT2 Inhibitors (STRONG)

Condition: Angina Patients With Non-obstructive Coronary Artery Disease · Coronary Microvascular Disease · Coronary Microvascular Dysfunction (CMD)  ·  Sponsor: University of Virginia

PhasePhase 1
Planned participants150
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

The goal of this clinical trial is to that Sodium-glucose cotransporter 2 inhibitors treatment will improve Coronary Microvascular Disease with anginal symptoms associated with non-obstructive coronary disease in women. The main questions it aims to answer are: Aim 1: Test the hypothesis that Sodium-glucose cotransporter 2 inhibitors treatment improves coronary microvascular disease in women with no evidence of epicardial obstructive coronary artery disease. Aim 2: Test the hypothesis that Sodium-glucose cotransporter 2 inhibitors treatment improves angina symptoms and other quality of life measurements associated with the improvement of CFR. AIM 3: Identify the effect of Sodium-glucose cotransporter 2 inhibition on inflammation pathways and markers of systemic Research will compare Brezavvy to placebo Participants will: * Take study drug or placebo for 12 weeks * Stress Cardiac magnetic resonance imaging * 12 lead electrocardiograms * Complete questionnaires

This description comes directly from the study's public registry record.

Talk to the study team

Patricia Rodriguez-Lozano, MD  ·  434-982-1058  ·  PR3GG@uvahealth.org

Shuo Wang  ·  4349821058  ·  VJR7CE@uvahealth.org

Always discuss trial participation with your own doctor first.

Locations (1)

UVA HealthCharlottesville, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06600178