CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 224 enrolled
Drug / intervention
pessary +1 moredevice
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/NCT02160314
NCT02160314N/ACompleted
CompareCT.gov

A Clinical Study to Assess the Safety of a Disposable Intra-vaginal Device for Stress Urinary Incontinence

Procter and Gamble·interventional·Posted Jun 10, 2014·Updated Feb 15, 2016

In Brief

A clinical study evaluating pessary and Absorbent pad for Stress Urinary Incontinence. Completed, enrolled 224 participants across 1 site.

Detailed Summary

This study will evaluate the safety of the pessary device by objective evaluation of vaginal wall integrity and subjective assessment of comfort during in-use conditions.

Study Details

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

Timeline

N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedJun 10, 2014
Enrollment StartMay 1, 2014
Primary CompletionJan 1, 2015
TodayJul 2, 2026
Enrollment to primary: 8 monthsPosted 12.1 years ago

Interventions

pessarydevice

disposable, single-use pessary

Absorbent paddevice