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NCT03782116 · ClinicalTrials.gov registry record · NA
Stress Incontinence Trial With Elitone Device
A NA study of Stress Urinary Incontinence, sponsored by Elidah.
- Completed
- Registry status
- NA
- Development phase
- 87
- Enrollment target
- 1
- Study location
NCT03782116 is a NA study of Stress Urinary Incontinence that has completed, run by Elidah. The registered enrollment target is 87 participants, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (46% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03782116, a NA study of Stress Urinary Incontinence, has completed, sponsored by Elidah.
- COMPLETED
- Registry status
- NA
- Development phase
- 87 participants
- Enrollment target
- 1
- Study location
Study 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.
Conditions Studied
Interventions
- DEVICE Transcutaneous electrical stimulation (Elitone)
Study Locations (1)
Connecticut
- Nationwide At-Home study - Monroe
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 87 participants |
| Start Date | 2018-09-01 |
| Est. Completion | 2019-03-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03782116
The ClinicalTrials.gov registry entry for NCT03782116 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 87 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (46% lower). The listed sponsor is Elidah, which has 4 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Stress Urinary Incontinence appearing as the primary indexed condition, and to 1 intervention - of which Transcutaneous electrical stimulation (Elitone) is the first listed.
NCT03782116 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.
Frequently Asked Questions
What is clinical trial NCT03782116 about?
NCT03782116 is a clinical study titled "Stress Incontinence Trial With Elitone Device". 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.
What is the current status of trial NCT03782116?
This trial is currently completed. It is a NA study. The enrollment target is 87 participants. The study started on 2018-09-01. Estimated completion is 2019-03-31.
What conditions does trial NCT03782116 study?
This clinical trial studies the following conditions: Stress Urinary Incontinence.
What interventions are being tested in trial NCT03782116?
The interventions under investigation include: Transcutaneous electrical stimulation (Elitone) (DEVICE).
Who is sponsoring clinical trial NCT03782116?
This trial is sponsored by Elidah, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03782116 being conducted?
This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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