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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

Sponsor: Stanford University · Participants: 9 · Started: Jul 10, 2021

Contact the study team

Official record on ClinicalTrials.gov — NCT04624126

Locations in the U.S.

CaliforniaStanford 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.