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NCT06840093 · ClinicalTrials.gov registry record · NA
Outcomes of Limited Postoperative Restrictions Following Sling Placement: A Randomized Controlled Trial
A NA study of Stress Urinary Incontinence and Postoperative Restriction, sponsored by University of Iowa.
- Recruiting
- Registry status
- NA
- Development phase
- 84
- Enrollment target
- 1
- Study location
NCT06840093: Recruiting NA study of Stress Urinary Incontinence and Postoperative Restriction, sponsored by University of Iowa.
NCT06840093 is a NA study of Stress Urinary Incontinence and Postoperative Restriction that is actively recruiting participants, run by University of Iowa. The registered enrollment target is 84 participants, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (47% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06840093, a NA study of Stress Urinary Incontinence and Postoperative Restriction, is actively recruiting participants, sponsored by University of Iowa.
- RECRUITING
- Registry status
- NA
- Development phase
- 84 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Primary Outcome
Questionnaire to assess the severity of lower urinary trat symptoms. Baseline compared to 3 months postoperatively with the hypothesis limited postoperative restrictions will result in non-inferior urinary symptoms compared to standard restrictions
Conditions Studied
Interventions
- BEHAVIORAL Limited Restrictions
- BEHAVIORAL Standard Restrictions
Study Locations (1)
Iowa
- University of Iowa Health Care - Iowa City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 84 participants |
| Start Date | 2025-03-01 |
| Est. Completion | 2027-06-30 |
| Phase | NA |
What NCT06840093 shows while recruiting
NCT06840093 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 84 participants, a relatively small participant target, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (47% lower).
The record links to 4 conditions, with Stress Urinary Incontinence appearing as the primary indexed condition, and to 2 interventions - of which Limited Restrictions is the first listed.
NCT06840093 reports a single indexed study location in Iowa.
Frequently Asked Questions
What is clinical trial NCT06840093 about?
NCT06840093 is a clinical study titled "Outcomes of Limited Postoperative Restrictions Following Sling Placement: A Randomized Controlled 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 wi...
What is the current status of trial NCT06840093?
This trial is currently recruiting. It is a NA study. The enrollment target is 84 participants. The study started on 2025-03-01. Estimated completion is 2027-06-30.
What conditions does trial NCT06840093 study?
This clinical trial studies the following conditions: Stress Urinary Incontinence, Postoperative Restriction, Midurethral Sling, Mesh.
What interventions are being tested in trial NCT06840093?
The interventions under investigation include: Limited Restrictions (BEHAVIORAL), Standard Restrictions (BEHAVIORAL).
Who is sponsoring clinical trial NCT06840093?
This trial is sponsored by University of Iowa, which has 228 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06840093 being conducted?
This trial has 1 study location across Iowa. 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 NCT06840093's enrollment target sits among peer trials
84 21st of 35 higher than 15 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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