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Study identifier: NCT06840093 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Outcomes of Limited Postoperative Restrictions Following Sling Placement: A Randomized Controlled Trial

Condition: Postoperative Restriction · Midurethral Sling · Mesh  ·  Sponsor: University of Iowa

PhaseNA
Planned participants84
Who can joinFemale, 18 Years to 99 Years
Healthy volunteersNo

About this study

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 and no lifting over 15lbs for six weeks after surgery. The other group will have fewer restrictions, with no restrictions on activity or lifting. Participants will complete surveys at 2 weeks, 3 months and 1 year following their procedure to help providers better understand how patients are following postoperative restrictions and if there were any differences in the outcome of the procedure between the two groups.

This description comes directly from the study's public registry record.

Talk to the study team

Leanne Brechtel, MD  ·  +1 319 356 2294  ·  leanne-brechtel@uiowa.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Iowa Health CareIowa City, Iowa, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06840093