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Активно (без набиране) NCT07479901

Investigation of the Effect of the Atherogenic Index on the Therapeutic Response to Tadalafil in Patients With Vascular Erectile Dysfunction

Заболявания: Erectile Dysfunction Vascular Erectile Dysfunction Atherogenic Dyslipidemia

Спонсор: Taksim Egitim ve Arastirma Hastanesi

Налично на: БГ
Обобщение
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.
Описание
The Atherogenic Index of Plasma (AIP) has been widely accepted as an indicator of atherogenic dyslipidemia and subclinical atherosclerosis. It is a simple laboratory-based parameter calculated using the formula log10 (triglycerides/HDL-C) and has been associated with increased cardiovascular risk. Vascular erectile dysfunction (VED) represents one of the most important organic causes of erectile dysfunction and results from vascular abnormalities that impair adequate penile blood flow. Tadalafil 5 mg administered once daily is an established treatment option for patients with vascular erectile dysfunction. However, the variability in treatment response suggests that underlying vascular risk factors may influence therapeutic outcomes. Identifying predictive biomarkers that can estimate treatment response may improve patient selection and treatment strategies. The primary objective of this study is to evaluate whether AIP levels are associated with the response to tadalafil treatment in patients with vascular erectile dysfunction. The study also aims to assess the relationship between lipid profile parameters and the severity of erectile dysfunction, as well as to identify potential predictors of treatment response. This study is designed as a prospective observational study. Participants diagnosed with vascular erectile dysfunction will receive tadalafil 5 mg once daily for a period of one month. Clinical and laboratory evaluations will be performed before and after treatment. The findings of this study are expected to determine whether AIP can serve as a potential biomarker for predicting the therapeutic response to tadalafil in patients with vascular erectile dysfunction.
Кой може да участва
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 \-
Места на провеждане 1
Турция (1)
Taksim Training and Research Hospital, Istanbul
Istanbul , beyoğlu
Технически детайли
Статус
Активно (без набиране)
Вид изследване
OBSERVATIONAL
Пол
Само мъже
Минимална възраст
40 Years
Здрави доброволци
Не
Начална дата
12.10.2025
Крайна дата
20.04.2026
Регистрационен номер
NCT07479901
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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