External Device for Erectile Dysfunction (3D-Erect)

Recruiting now · Not applicable

Conditions studied: Erectile Dysfunction, Impotentia Erigendi

In brief

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).

Key facts

Study ID

NCT04624126

Run by

Stanford University

People needed

9

Starts

2021-07-10

Expected to finish

2026-12-01

Last updated by the study team

2026-01-13

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• not willing to attempt sexual vaginal intercourse with their partner
• inability to wear/operate the external penile device for any reason

Where it is running

• Stanford Health Care, Stanford Hospital — Stanford, California, United States (enrolling)

Full record on ClinicalTrials.gov

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