RecruitingNot ApplicableNCT04624126
External Device for Erectile Dysfunction (3D-Erect)
Non-invasive External Device for Erectile Dysfunction (3D-Erect): a Pilot Study
Sponsor
Stanford University
Enrollment
9 participants
Start Date
Jul 10, 2021
Study Type
INTERVENTIONAL
Conditions
Summary
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).
Eligibility
Sex: MALEMin Age: 18 Years
Inclusion Criteria2
- 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 Criteria2
- 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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Interventions
DEVICE3D-Erect
3D-printed erectile device for intercourse
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT04624126
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