At a glance
ClinicalIndex Comparison RecordN/ACompleted· 87 enrolled
Drug / intervention
Transcutaneous electrical stimulation (Elitone)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.
Randomized Controlled Study of Efficacy of Elitone Device For the Treatment of Mild-Moderate Stress Urinary Incontinence
In Brief
A clinical study evaluating Transcutaneous electrical stimulation (Elitone) for Stress Urinary Incontinence. Completed, enrolled 87 participants across 1 site.
Detailed Summary
This is a randomized controlled study in which subjects are assigned to either a treatment group or a control (sham) group. Pre- and post-study outcome measures evaluate the change in incontinence episodes on women with mild-moderate stress urinary incontinence.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsStress Urinary Incontinence
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
Enrollment StartSep 2018
First PostedDec 2018
Primary CompletionMar 2019
TodayJul 2026
First PostedDec 20, 2018
Enrollment StartSep 1, 2018
Primary CompletionMar 31, 2019
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 7.5 years ago
Interventions
Transcutaneous electrical stimulation (Elitone)device
Transcutaneous perineal area electrical stimulation