CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 148 enrolled
Drug / intervention
pessary (disposable intra-vaginal device)device
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01762345
NCT01762345N/ACompleted
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A Pilot Clinical Study of the Efficacy and Safety of a Disposable Intravaginal Device for Stress Urinary Incontinence

Procter and Gamble·interventional·Posted Jan 7, 2013·Updated Mar 24, 2016

In Brief

A clinical study evaluating pessary (disposable intra-vaginal device) for Stress Urinary Incontinence. Completed, enrolled 148 participants across 1 site.

Detailed 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).

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsStress Urinary Incontinence
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedJan 7, 2013
Enrollment StartDec 1, 2012
Primary CompletionJul 1, 2013
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 13.5 years ago

Interventions

pessary (disposable intra-vaginal device)device

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