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NCT02617472 · ClinicalTrials.gov registry record · NA
Effectiveness of Kegel Exercise Device in Strengthening Pelvic Floor and Treating Urinary Incontinence (UI)
A NA study of Stress Urinary Incontinence and Sexual Dysfunction, sponsored by Lelo.
- Completed
- Registry status
- NA
- Development phase
- 93
- Enrollment target
- 1
- Study location
NCT02617472 is a NA study of Stress Urinary Incontinence and Sexual Dysfunction that has completed, run by Lelo. The registered enrollment target is 93 participants, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (42% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02617472, a NA study of Stress Urinary Incontinence and Sexual Dysfunction, has completed, sponsored by Lelo.
- COMPLETED
- Registry status
- NA
- Development phase
- 93 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will assess the effectiveness of a new pelvic floor exercise device in strengthening pelvic floor muscles and treating urinary incontinence among women who are experiencing symptoms of pelvic floor weakness. The study will be conducted over 12 weeks and results will be collected through self-assessment questionnaires and clinical pelvic examination. Effectiveness outcomes will be tracked over the duration of the trial and measured against historical symptoms.
Conditions Studied
Interventions
- DEVICE Pelvic floor exerciser
Study Locations (1)
Arizona
- Banner University Medical Center - Phoenix
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 93 participants |
| Start Date | 2015-11 |
| Est. Completion | 2017-08 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02617472
The ClinicalTrials.gov registry entry for NCT02617472 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 93 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 (42% lower). The listed sponsor is Lelo, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Stress Urinary Incontinence appearing as the primary indexed condition, and to 1 intervention - of which Pelvic floor exerciser is the first listed.
NCT02617472 reports 1 study location spanning 1 distinct geographic area - top geographies include Arizona.
Frequently Asked Questions
What is clinical trial NCT02617472 about?
NCT02617472 is a clinical study titled "Effectiveness of Kegel Exercise Device in Strengthening Pelvic Floor and Treating Urinary Incontinence (UI)". This study will assess the effectiveness of a new pelvic floor exercise device in strengthening pelvic floor muscles and treating urinary incontinence among women who are experiencing symptoms of pelvic floor weakness. The study will be conducted over 12 weeks and results will be collected through s...
What is the current status of trial NCT02617472?
This trial is currently completed. It is a NA study. The enrollment target is 93 participants. The study started on 2015-11. Estimated completion is 2017-08.
What conditions does trial NCT02617472 study?
This clinical trial studies the following conditions: Stress Urinary Incontinence, Sexual Dysfunction.
What interventions are being tested in trial NCT02617472?
The interventions under investigation include: Pelvic floor exerciser (DEVICE).
Who is sponsoring clinical trial NCT02617472?
This trial is sponsored by Lelo, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02617472 being conducted?
This trial has 1 study location across Arizona. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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