The utility of penile compression device for the quality of life in Male urinary incOntinence after pRostatEctomy: A randomized prospective study

The utility of penile compression device for the quality of life in Male urinary incOntinence after pRostatEctomy: A randomized prospective study - The MORE study

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000030684

Enrollment

Registered

2018-03-15

Start date

2018-03-26

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

Male urinary incOntinence after prostatectomy

Interventions

Use of the penile compression device for 28 days except at bedtime No use of the penile compression device

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Patients who suffer from stress urinary incontinence after prostatectomy

Exclusion criteria

Exclusion criteria: - Less than a month after prostatectomy - Severe disease of penile skin - After the implantation of artificial urinary sphincter

Design outcomes

Primary

Measure	Time frame
Changes of King's Health Questionnaire scores	—

Secondary

Measure	Time frame
Changes in the number of urine pads used per day Changes in the weight of urine pads per day	—

Countries

Japan

Contacts

Public ContactKazumasa Torimoto

Nara Medical University Department of Urology

torimoto@naramed-u.ac.jp0744-22-3051

Outcome results

None listed

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