Investigation of the efficacy of autologous platelet-rich plasma administration on the potency of patients with vasculogenic and/or neurogenic erectile dysfunction
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
34
intracavernous platelet-rich plasma therapy for erectile dysfunction
University of Health Sciences, Bakırköy Sadi Konuk Training and Research Hospital
Istanbul, Istanbul, Turkey (Türkiye)
IIEF
To observe the increase in the International Index of Erectile Function (IIEF) score after treatment compared to before treatment in patients.
Time frame: 6 months
FSFI
To observe FSFI score increases in patients' partners before and after treatment using the Female Sexual Function Inventory (FSFI).
Time frame: 6 months
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