Recruitment

Recruitment Status
Active, not recruiting
Estimated Enrollment
Same as current

Summary

Conditions
Urinary Incontinence
Type
Interventional
Phase
Phase 1
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Double (Participant, Investigator)Primary Purpose: Treatment

Participation Requirements

Age
Between 50 years and 80 years
Gender
Only males

Description

Aim: To determine the effect of sildenafil on urinary incontinence. Episodes of urinary incontinence will be recorded using a 3 day bladder diary. Quantitative assessment of urinary incontinence will be performed at baseline and after treatment using a Pad Test. Muscle strength will be assessed thro...

Aim: To determine the effect of sildenafil on urinary incontinence. Episodes of urinary incontinence will be recorded using a 3 day bladder diary. Quantitative assessment of urinary incontinence will be performed at baseline and after treatment using a Pad Test. Muscle strength will be assessed through use of a perineometer. To evaluate macrocirculatory blood flow in pelvic organs, women will be assessed with noninvasive imaging before and after randomization to sildenafil. Secondary outcomes will include evaluation of muscle and vaginal mucosal thickness.

Tracking Information

NCT #
NCT02983461
Collaborators
Not Provided
Investigators
Principal Investigator: Kathleen L Vincent, MD University of Texas