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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 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.
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.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06840093
The ClinicalTrials.gov registry entry for NCT06840093 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 84 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 160-participant average among 35 other Stress Urinary Incontinence trials with a reported enrollment target (47% lower). The listed sponsor is University of Iowa, which has 228 total studies on file at ClinicalTrials.gov.
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 1 study location spanning 1 distinct geographic area - top geographies include 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.
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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.