Urological and Genital Diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Male participants aged 19–64 years Diagnosed with vasculogenic erectile dysfunction Stable heterosexual relationship for at least 3 months No ED treatment in the previous 6 months Willing and able to provide written informed consent Regular sexual activity (at least once weekly)
Exclusion criteria
Exclusion criteria: Peyronie’s disease or significant penile deformity ED due to neurogenic, hormonal, or psychogenic causes Use of psychotropic drugs, antipsychotics, or antihypertensives affecting sexual function Active malignancy, autoimmune disease, or coagulopathy Abnormal hormonal profile (FSH, LH, or prolactin) Previous penile surgery or trauma Contraindications to PRP or tadalafil therapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in cavernosal C-reactive protein (CRP) and fibrinogen levels | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary Outcome 1 Change in International Index of Erectile Function-5 (IIEF-5) score ;Secondary Outcome 1 Outcome Type: ? Secondary Outcome Outcome: Change in International Index of Erectile Function-5 (IIEF-5) score Time point(s) at which outcome measured: Baseline and 6 weeks post-treatment Change in penile duplex Doppler parameters (peak systolic velocity, end-diastolic velocity, resistive index) | — |
Countries
Egypt
Contacts
Professor Al Azhar University