Non-invasive External Device for Erectile Dysfunction (3D-Erect): a Pilot Study
Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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).
Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:
• 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.
Locations
United States
California
Stanford Health Care, Stanford Hospital
RECRUITING
Stanford
Time Frame
Start Date: 2021-07-10
Estimated Completion Date: 2025-12
Participants
Target number of participants: 9
Treatments
Experimental: 3D-Erect arm
Participants will be asked to use the 3D-printed penile device during their intercourse with partners.
Related Therapeutic Areas
Sponsors
Leads: Stanford University