This study aims to investigate the relationship between the atherogenic index of plasma (AIP) and the therapeutic response to daily tadalafil 5 mg treatment in patients diagnosed with vascular erectile dysfunction (VED). AIP is considered a marker of atherogenic dyslipidemia and subclinical atherosclerosis and is calculated using the formula log10 (triglycerides/HDL-C). Since vascular abnormalities play a major role in the pathophysiology of erectile dysfunction, AIP may reflect underlying vascular risk and potentially predict treatment outcomes. In this prospective observational study, patients with vascular erectile dysfunction will receive tadalafil 5 mg once daily for one month, and treatment response will be evaluated by comparing clinical parameters before and after therapy.
Who can participate
Age range
40 Years
Sex
MALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:Men older than 40 years of age who have been diagnosed with vascular erectile dysfunction, have had symptoms for at least three months, have been considered suitable for tadalafil treatment, and have received tadalafil therapy for at least four weeks.
\-
Exclusion Criteria:Use of nitrates
Uncontrolled cardiac arrhythmias
Hypotension
Diagnosis of hypogonadism
History of major cardiovascular events within the last 6 months (including uncontrolled hypertension or severe ischemic heart disease)
Severe hepatic or renal insufficiency
Patients receiving hormone replacement therapy
Patients diagnosed with psychogenic, neurological, hormonal, or pharmacological erectile dysfunction
History of radical pelvic surgery
Anatomical abnormalities of the penis
History of non-arteritic anterior ischemic optic neuropathy (NAION)
Retinitis pigmentosa
Known hypersensitivity to tadalafil or other phosphodiesterase type-5 inhibitors
Alcohol or substance abuse
Use of other treatments for erectile dysfunction
Unstable diabetes mellitus
History of medications affecting lipid profile (such as corticosteroids or certain antidepressants)
Initiation or dose modification of lipid-lowering therapy (e.g., statins, fibrates) within the last 3 months
Uncontrolled thyroid dysfunction
Active infection or inflammatory conditions
Patients receiving active cancer treatment
Inability to comply with study procedures
Beck Depression Inventory score greater than 0
\-
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Association Between Atherogenic Index of Plasma and Response to Tadalafil Treatment