Does Erectile Dysfonction Allow to Evaluate Subendocardial Viability Among Treated Patients With Hypertension ?
- Sponsor
- Assistance Publique - Hôpitaux de Paris
- Study ID
- NCT07719790
- Status
- Not Yet Recruiting
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Conditions
- Erectile Dysfunction
- Hypertension
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Study Details
Erectile dysfunction (ED) is associated with subclinical atherosclerosis and may precede clinically apparent coronary artery disease by two to five years. It may therefore serve as an early warning sign of cardiovascular disease and help identify patients who could benefit from intensified cardiovascular risk-factor management. The subendocardial viability ratio (SEVR), also known as the Buckberg index, is obtained noninvasively from radial artery applanation tonometry. SEVR reflects the balance between myocardial oxygen supply and demand and has been associated with coronary flow reserve in patients with hypertension. The DEVISE study will compare SEVR between treated men with hypertension who have ED with those who do not. The study will also examine the associations between ED severity and arterial stiffness, central hemodynamics, exercise capacity, left ventricular mass, coronary artery calcium, high-sensitivity C-reactive protein, cardiovascular risk, and quality of life. The question addressed in our study is whether an alteration in subendocardial viability represents subclinical coronary disease associated with ED.
Key Dates
- First listed
- Jul 22, 2026
- Start date
- Jul 17, 2026
- Status verified
- Jul 2026
- Primary completion
- Jan 17, 2028
- Completion
- Jan 17, 2028
Study Design
- Enrollment
- 120 participants (estimated)
Arms
- Arm: Treated hypertensive men with erectile dysfunctionTreated hypertensive men without erectile dysfunction
- Arm: Patients with hypertension without erectile dysfunction
Primary Outcome Measure
Subendocardial viability ratio (SEVR) [ Time Frame: Once, during the day-hospital visit ]
Central Contacts
- Guy AMAH, MD0149958088
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