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 — DEVICE
    3D-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 arm
    Participants 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)

FacilityCityStateZIPSite coordinators
Stanford Health Care, Stanford HospitalStanfordCalifornia94305
Satvir Basran
(650) 723-0948
Francesco Del Giudice, MD (SUB_INVESTIGATOR)
Tony Chen, MD (SUB_INVESTIGATOR)
Alex M Kasman, MD (SUB_INVESTIGATOR)

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