NCT04624126NARecruiting
External Device for Erectile Dysfunction (3D-Erect)
Stanford University
Start Date
7/10/2021
Completion Date
12/1/2026
Summary
The aim of this clinical trial is to test the safety and feasibility of a non-invasive 3D-printed external penile device to achieve successful and satisfactory sexual intercourse in men with erectile dysfunction (ED).
Detailed Description
A clinical trial to test the safety and feasibility of our newly developed non-invasive 3D-printed external penile device for the treatment and recovery of erectile dysfunction.
Eligibility Criteria
Age Range: 18 years to No maximum
Inclusion Criteria:
* males \>18 years old suffering from any cause moderate to severe erectile dysfunction (e.g. ED after radical prostatectomy and/or radiation therapy for prostate cancer and or other pelvic malignancies affecting the sexual potency; emotional and psychological ED; organic vascular and/or metabolic ED etc.)
* having a female partner willing to participate in the study.
Exclusion Criteria:
* not willing to attempt sexual vaginal intercourse with their partner
* inability to wear/operate the external penile device for any reason
Interventions
DEVICE
3D-Erect
Conditions
Erectile DysfunctionImpotentia Erigendi
Locations
Stanford Health Care, Stanford Hospital
Stanford, California 94305
United States