Fundus Oculi and Erectile Dysfunction (NCT02845765) | Clinical Trial Compass
UnknownNot Applicable
Fundus Oculi and Erectile Dysfunction
Italy60 participantsStarted 2016-02
Plain-language summary
The purpose of this study is to evaluate the correlation between fundus oculi's vascularization in patients with erectile dysfunction and not, and, in the same patients, before and after using drugs for ED.
Who can participate
Age range40 Years – 60 Years
SexMALE
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Inclusion Criteria:
* Subjects with erectile dysfunction diagnosis (organic and psychogenic);
* Subjects with Erectile Dysfunction diagnosis defined by IIEF score ≤ 25
* Subjects with stable partner for at least 6 months and sexually active.
* Subjects aged between 40 - 60 years;
* Signature of informed consent for patients
Exclusion Criteria:
* Subjects with ED secondary diagnosis to hormonal alterations (i.e. hypogonadism, hypo / hyperthyroidism, hyperprolactinemia);
* Subjects with a diagnosis of ED post-traumatic and iatrogenic, since after pelvic surgery;
* Subjects suffering from any ocular pathology that involves use of contact lenses and / or glasses;
* Subjects smoking;
* Individuals with uncontrolled systemic diseases;
* All persons who do not confirm at least one criterion for inclusion.