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NCT06698627 · ClinicalTrials.gov registry record · NA
Comparison of Two Over the Counter Intravaginal Devices for the Treatment of Stress Urinary Incontinence
A NA study, sponsored by Vanderbilt University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 60
- Enrollment target
NCT06698627 is a NA study that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 60 participants.
The verdict
NCT06698627, a NA study, has completed, sponsored by Vanderbilt University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 60 participants
- Enrollment target
Study Summary
The goal of this pilot study is to compare two commercially available over the counter devices for treatment of stress urinary incontinence in a web based format. The main questions it aims to answer 1. What device do women with SUI prefer after using both devices 2. What patient factors help drive this preference if any 3. Is a web-based crossover intervention study feasible Participants will: Use two over the counter devices over a course of 20 days. They will have both devices sent via mail. They will answer questions prior to the start of using any device and then after using each device They will be asked to complete daily bladder diaries
Interventions
- DEVICE Daily Disposable Continence Device
- DEVICE Monthly Disposable Continence Device
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 60 participants |
| Start Date | 2025-06-30 |
| Est. Completion | 2026-06-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06698627
The ClinicalTrials.gov registry entry for NCT06698627 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 60 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Daily Disposable Continence Device is the first listed.
NCT06698627 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT06698627 about?
NCT06698627 is a clinical study titled "Comparison of Two Over the Counter Intravaginal Devices for the Treatment of Stress Urinary Incontinence". The goal of this pilot study is to compare two commercially available over the counter devices for treatment of stress urinary incontinence in a web based format. The main questions it aims to answer 1. What device do women with SUI prefer after using both devices 2. What patient factors help driv...
What is the current status of trial NCT06698627?
This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2025-06-30. Estimated completion is 2026-06-01.
What interventions are being tested in trial NCT06698627?
The interventions under investigation include: Daily Disposable Continence Device (DEVICE), Monthly Disposable Continence Device (DEVICE).
Who is sponsoring clinical trial NCT06698627?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
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