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Prostate Stimulation for Sexual Dysfunction

Not Applicable
Recruiting
Conditions
Erectile Dysfunction
Anorgasmia
Delayed Ejaculation
Sexual Dysfunction
Interventions
Device: Prostate stimulator
Registration Number
NCT05468931
Lead Sponsor
Stanford University
Brief Summary

The purpose of this study is to use a device to stimulate the prostate with a goal of helping improve symptoms in men with sexual dysfunction.

Detailed Description

The purpose of the study is to use a device to stimulate the prostate. The goal of this is to help men with sexual dysfunction. Sexual dysfunction can include conditions like delayed ejaculation (e.g.takes more than 21 minutes to climax) and can hopefully assist them in achieving faster time to ejaculation (e.g. closer to the median of 5.4 minutes in a "normal" individual) along with erectile dysfunction (e.g. the inability to achieve and sustain an erection).

Recruitment & Eligibility

Status
RECRUITING
Sex
Male
Target Recruitment
15
Inclusion Criteria
  • Males >18 years of age suffering from sexual dysfunction
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Exclusion Criteria
  • Individuals who have had a prostatectomy - removal of prostate
  • Inability to operate the device for any reason
  • Females
  • Males <18 years of age
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Prostate stimulation device armProstate stimulatorParticipants will be asked to use our prostate stimulation device.
Primary Outcome Measures
NameTimeMethod
change in modified International Index of Erectile Dysfunction scorebaseline and up to 1 month post-baseline

score 0 to 30 with higher score meaning better erectile function

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Stanford Healthcare, Stanford Hospital

🇺🇸

Stanford, California, United States

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