The purpose of this study is to determine whether spironolactone reduces aortic stiffness, measured by carotid-femoral pulse wave velocity (cfPWV), compared with placebo, in patients with degenerative thoracic aortic aneurysms.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
50
Subjects will receive spironolactone 25 mg once daily for the first 4 weeks, followed by an increased dose of 50 mg once daily for an additional 5 months.
Subjects will receive 25 mg of the placebo once daily for the first 4 weeks, followed by an increased dose of 50 mg once daily for an additional 5 months.
Mayo Clinic in Rochester
Rochester, Minnesota, United States
RECRUITINGChange in Carotid-femoral pulse wave velocity (cfPWV)
Carotid-femoral pulse wave velocity will be calculated by (Distance/Pulse Transit Time) and reported as m/s
Time frame: Baseline, 6 months
Changes in central blood pressure
Central blood Pressure will be measured using a electronic sphygmomanometer and reported as mmHg
Time frame: Baseline, 6 months
Aortic characteristic impedance
Aortic characteristic impedance will be reported as a ratio of increase in central pressure to the corresponding increase in aortic flow in early systole
Time frame: Baseline, 6 months
Total and proximal arterial compliance
Change in artery diameter (millimeter) assessed via ultrasound per change in artery pressure (mm Hg) assessed via tonometry.
Time frame: Baseline, 6 months
Indices of wave reflection
Aortic Wave Reflection will be measured via arterial tonometry, reported as aortic augmentation index
Time frame: Baseline, 6 months
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