Investigation of the efficacy of autologous platelet-rich plasma administration on the potency of patients with vasculogenic and/or neurogenic erectile dysfunction
Eligibility
Sex
MALE
Min age
40 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria:
\- 1)40-70 years old male, sexually active heterosexual, 2) Patients with a diagnosis of mild to moderate erectile dysfunction (IIEF score between 8-21) according to the International Index of Erectile Function (IIEF) for at least 3 months, 3) Patients who cannot achieve an erection despite peroral PDE5 inhibitor and intracavernous alprostadil injection therapy
Exclusion Criteria:
1. Patients with psychogenic erectile dysfunction, 2) Patients with a history of priapism, penile fracture, peyronie, penile curvature 3) Patients with a history of radical prostatectomy, 4) Patients with a history of major pelvic trauma, surgery, radiotherapy, 5) Patients with a history of malignancy affecting survival, 6) Patients with severe psychiatric illness that impairs adherence to treatment, 7) Patients with any bleeding disorder or on anti-aggregants/coagulants.
Primary outcome measure(s)
IIEF — 6 months To observe the increase in the International Index of Erectile Function (IIEF) score after treatment compared to before treatment in patients.
Trial sites (1)
Facility
City
Region
Status
University of Health Sciences, Bakırköy Sadi Konuk Training and Research Hospital
Istanbul
Istanbul
More Bakirkoy Dr. Sadi Konuk Research and Training Hospital trials in Turkey
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
We use cookies to analyse site traffic and improve your experience. With your consent, we may also use cookies for advertising. You can change your choice at any time.