External Device for Erectile Dysfunction (3D-Erect)

Trial ID or NCT#

NCT04624126

Status

recruiting iconRECRUITING

Purpose

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).

Official Title

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

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: Male
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. - 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:
  1. - not willing to attempt sexual vaginal intercourse with their partner - inability to wear/operate the external penile device for any reason
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Investigator(s)

Tony Chen, MD
Tony Chen, MD
Clinical Assistant Professor, Urology
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View on ClinicalTrials.gov