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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: Recruiting NA study of Stress Urinary Incontinence, sponsored by Cedars-Sinai Medical Center.
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. According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Return to normal activity immediately after mid-urethral sling surgery could result in faster return to baseline health-related quality of life. Each questionnaire will be administered weekly following surgery until the patient returns to within 10% of baseline scores. Cost-effectiveness of early return to normal activity via Productivity Loss form as time spent recovering from surgery will be analyzed (incremental cost effectiveness ratio of net means by comparing the unrestricted and restricte
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 |
What NCT02316275 shows while recruiting
NCT02316275 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 161-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (69% lower).
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 a single indexed study location in 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
Similar trials for Stress Urinary Incontinence
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02316275's enrollment target sits among peer trials
50 29th of 35 higher than 6 of 35 other Stress Urinary Incontinence trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Stress Urinary Incontinence trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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