The purpose of this study is to use a minimally invasive erectile device for patients suffering from erectile dysfunction.
The purpose of the study is to use a minimally invasive erectile device support to provide to patients suffering from erectile dysfunction the possibility to achieve satisfactory penetrating intercourse. The goal of this is to help men who have issues with erectile function (e.g.after radical prostatectomy for prostate cancer, vascular or metabolic erectile dysfunction non-responsive to phosphodiesterase-5 inhibitor medications, etc.) to have medication-free mechanical support for their penis in order to obtain sexual penetration satisfactorily.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
OTHER
Masking
NONE
Enrollment
10
Wearable device for intercourse
Stanford Healthcare, Stanford Hospital
Stanford, California, United States
RECRUITINGChange in modified International Index of Erectile Dysfunction score
score 0 to 30 with higher score meaning better erectile function
Time frame: baseline and up to 1 month post-baseline
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