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Study identifier: NCT04624126 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting3D-Erect

External Device for Erectile Dysfunction (3D-Erect)

Condition: Erectile Dysfunction · Impotentia Erigendi  ·  Sponsor: Stanford University

PhaseNA
Planned participants9
Who can joinMale, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
WhereStanford, California, United States

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this 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).

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

There is no obligation to join — the study team can answer your questions about taking part.

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Full eligibility criteria (exactly as the study team wrote them)

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

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (1)

Stanford Health Care, Stanford HospitalStanford, California, United StatesRecruiting

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Stanford

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