Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05451563

Double-S: a Wearable Device for Erectile Dysfunction

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
10 (estimated)
Sponsor
Stanford University · Academic / Other
Sex
Male
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to use a minimally invasive erectile device for patients suffering from erectile dysfunction.

Detailed description

The purpose of the study is to use a minimally invasive erectile device support to provide to patients suffering from erectile dysfunction the possibility to achieve satisfactory penetrating intercourse. The goal of this is to help men who have issues with erectile function (e.g.after radical prostatectomy for prostate cancer, vascular or metabolic erectile dysfunction non-responsive to phosphodiesterase-5 inhibitor medications, etc.) to have medication-free mechanical support for their penis in order to obtain sexual penetration satisfactorily.

Conditions

Interventions

TypeNameDescription
DEVICEDouble-SWearable device for intercourse

Timeline

Start date
2024-03-21
Primary completion
2026-06-01
Completion
2026-06-01
First posted
2022-07-11
Last updated
2025-05-22

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05451563. Inclusion in this directory is not an endorsement.