External Device for Erectile Dysfunction (3D-Erect)
Trial ID or NCT#
NCT04624126
Status
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:
- * 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
Investigator(s)
View on ClinicalTrials.gov