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External Device for Erectile Dysfunction (3D-Erect)
Recruiting
Non-invasive External Device for Erectile Dysfunction (3D-Erect): a Pilot Study
Who can join
Ages 18 and older · Men
Full eligibility criteria
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
About the study
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).
What is being tested
- 3D-Erect (device)
Sponsor: Stanford University · Participants: 9 · Started: Jul 10, 2021
Contact the study team
Official record on ClinicalTrials.gov — NCT04624126
Locations in the U.S.
| California | Stanford Health Care, Stanford Hospital, Stanford |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.