External Device for Erectile Dysfunction (3D-Erect)
Part of paid clinical trials in Stanford, California.
- Sponsor
- Stanford University
- Study ID
- NCT04624126
- Status
- Recruiting
Conditions
- Erectile Dysfunction
- Impotentia Erigendi
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- 3D-Erect — DEVICE3D-printed erectile device for intercourse
Study Details
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 Dates
- Start date
- Jul 10, 2021
- Status verified
- Jan 2026
- Primary completion
- Dec 31, 2026
- Completion
- Dec 31, 2026
Study Design
- Enrollment
- 9 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- DEVICE_FEASIBILITY
Arms
- Experimental: 3D-Erect armParticipants will be asked to use the 3D-printed penile device during their intercourse with partners.
Primary Outcome Measure
Change in modified International Index of Erectile Dysfunction score [ Time Frame: baseline and up to 1 month post-baseline ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Stanford Health Care, Stanford Hospital | Stanford | California | 94305 | Francesco Del Giudice, MD (SUB_INVESTIGATOR) Tony Chen, MD (SUB_INVESTIGATOR) Alex M Kasman, MD (SUB_INVESTIGATOR) |
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