Clinical Trials Directory

Trials / Completed

CompletedNCT01762345

A Pilot Clinical Study of the Efficacy and Safety of a Disposable Intravaginal Device for Stress Urinary Incontinence

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
148 (actual)
Sponsor
Procter and Gamble · Industry
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This pilot study will evaluate the efficacy of the pessary (disposable intra-vaginal device) by reduction in urine leakage in women with stress urinary incontinence (SUI).

Conditions

Interventions

TypeNameDescription
DEVICEpessary (disposable intra-vaginal device)pessary device(disposable intra-vaginal device)manufactured by Procter \& Gamble

Timeline

Start date
2012-12-01
Primary completion
2013-07-01
Completion
2013-07-01
First posted
2013-01-07
Last updated
2016-03-24
Results posted
2016-03-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01762345. Inclusion in this directory is not an endorsement.

A Pilot Clinical Study of the Efficacy and Safety of a Disposable Intravaginal Device for Stress Urinary Incontinence (NCT01762345) · Clinical Trials Directory