Outcomes of Limited Postoperative Restrictions Following Sling Placement: A Randomized Controlled Trial
Recruiting
N/A
Interventional Study
Postoperative Restriction
Midurethral Sling
Mesh
Stress Urinary Incontinence
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 99
- Sex
- Female
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 84 (estimated)
- Sponsor
- University of Iowa · Other
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About This Trial
The purpose of this research study is to better understand optimal restrictions for patients postoperatively following a mesh urethral sling placement for patients with stress urinary incontinence.
Patients undergoing a midurethral sling procedure will be assigned to one of two groups. One group with be given standard postprocedural restrictions including instructions to avoid moderate activity a…
Trial Locations
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Eligibility Criteria
Inclusion: Undergoing isolated synthetic mesh retropubic midurethral sling placement Exclusion criteria: Non-English speaking, incarcerated, cognitive impairment precluding informed consent, unable to ambulate without the assistance of an ambulation device, concurrent prolapse procedure
Contacts