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NCT02316275 · ClinicalTrials.gov registry record · NA
Impact of Unrestrictive Exercise Following Mid-Urethral Sling Surgery
A NA study of Stress Urinary Incontinence, sponsored by Cedars-Sinai Medical Center.
- Recruiting
- Registry status
- NA
- Development phase
- 50
- Enrollment target
- 1
- Study location
NCT02316275 is a NA study of Stress Urinary Incontinence that is actively recruiting participants, run by Cedars-Sinai Medical Center. The registered enrollment target is 50 participants, below the 161-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (69% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02316275, a NA study of Stress Urinary Incontinence, is actively recruiting participants, sponsored by Cedars-Sinai Medical Center.
- RECRUITING
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
- 1
- Study location
Study Summary
To determine the impact of unrestricted postoperative activity on intermediate- and long-term continence outcomes of mid-urethral sling surgery in women with stress urinary incontinence. To assess the natural return to baseline activity level when patients are unrestricted following mid-urethral sling surgery with or without concomitant anterior or posterior pelvic organ prolapse repair.
Conditions Studied
Interventions
- OTHER No post-operative activity restrictions
- OTHER Standard post-operative activity restriction
Study Locations (1)
California
- Cedars-Sinai Medical Center - Beverly Hills
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2011-12 |
| Est. Completion | 2031-12 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02316275
The ClinicalTrials.gov registry entry for NCT02316275 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 161-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (69% lower). The listed sponsor is Cedars-Sinai Medical Center, which has 339 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 2 interventions - of which No post-operative activity restrictions is the first listed.
NCT02316275 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT02316275 about?
NCT02316275 is a clinical study titled "Impact of Unrestrictive Exercise Following Mid-Urethral Sling Surgery". To determine the impact of unrestricted postoperative activity on intermediate- and long-term continence outcomes of mid-urethral sling surgery in women with stress urinary incontinence. To assess the natural return to baseline activity level when patients are unrestricted following mid-urethral sl...
What is the current status of trial NCT02316275?
This trial is currently recruiting. It is a NA study. The enrollment target is 50 participants. The study started on 2011-12. Estimated completion is 2031-12.
What conditions does trial NCT02316275 study?
This clinical trial studies the following conditions: Stress Urinary Incontinence.
What interventions are being tested in trial NCT02316275?
The interventions under investigation include: No post-operative activity restrictions (OTHER), Standard post-operative activity restriction (OTHER).
Who is sponsoring clinical trial NCT02316275?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02316275 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.