Validation test of the new penile tumescence and stiffness monitoring device

Validation test of the new penile tumescence and stiffness monitoring device - Validation test of the new penile tumescence and stiffness monitoring device

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000037049

Enrollment

Registered

2019-06-13

Start date

2019-04-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Erectile Dysfunction

Interventions

The new penile tumescence and stiffness monitoring device

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Agreed to take a measurement of penile stifness using the new device (Irrepective of the presence of erectile dysfunction)

Exclusion criteria

Exclusion criteria: Patients whom the physician considered inappropriate for this study.

Design outcomes

Primary

Measure	Time frame
Can the new device measure nocturnal penile tumescence?	—

Countries

Japan

Contacts

Public ContactSeiji Matsumoto

Asahikawa Medical University Center for Advanced Research and Education

matsums@asahikawa-med.ac.jp0166-68-2618

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026