External Device for Erectile Dysfunction (3D-Erect)

Description

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).

Conditions

Erectile Dysfunction, Impotentia Erigendi

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Study Overview

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Study Details

Study overview

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).

Non-invasive External Device for Erectile Dysfunction (3D-Erect): a Pilot Study

External Device for Erectile Dysfunction (3D-Erect)

Condition
Erectile Dysfunction
Intervention / Treatment

-

Contacts and Locations

Stanford

Stanford Health Care, Stanford Hospital, Stanford, California, United States, 94305

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

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

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

MALE

Accepts Healthy Volunteers

No

Collaborators and Investigators

Stanford University,

Michael Eisenberg, MD, PRINCIPAL_INVESTIGATOR, Stanford University

Study Record Dates

2025-06