MedPath

Validation test of the new penile tumescence and stiffness monitoring device

Not Applicable
Conditions
Erectile Dysfunction
Registration Number
JPRN-UMIN000037049
Lead Sponsor
Asahikawa Medical University
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
Male
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

Patients whom the physician considered inappropriate for this study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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