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NCT02400034 · ClinicalTrials.gov registry record · NA
Comparing Voiding Trials After Midurethral Sling for Stress Incontinence
A NA study, sponsored by Northwell Health.
- Completed
- Registry status
- NA
- Development phase
- 112
- Enrollment target
NCT02400034: Completed NA study, sponsored by Northwell Health.
NCT02400034 is a NA study that has completed, run by Northwell Health. The registered enrollment target is 112 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02400034, a NA study, has completed, sponsored by Northwell Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 112 participants
- Enrollment target
Study Summary
Urinary incontinence is a prevalent health and quality of life concern affecting almost half of women over the age of 20. Urinary retention (abnormal holding of urine) is a concern of many surgeons who perform midurethral sling surgery. All patients after outpatient midurethral sling or vaginal prolpase surgery must complete a voiding trial if they are to be discharged without a catheter. The purpose of this study is to compare two different types of postoperative voiding trials to determine which leads to less post-operative issues, such as urinary retention requiring catheterization. You are being asked to participate because you are having midurethral sling surgery, either with or without vaginal prolapse repair.
Primary Outcome
Any additional visit outside the patient's scheduled postoperative visits to the emergency room, urgent care facility or doctor's office will be recorded for up to 6 six weeks postoperatively
Interventions
- OTHER Voiding trial
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 112 participants |
| Start Date | 2015-03 |
| Est. Completion | 2016-06 |
| Phase | NA |
What the finished NCT02400034 record still lists
NCT02400034 is an interventional study that assigns participants to a tested intervention. The registered 112 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 1 intervention - of which Voiding trial is the first listed.
NCT02400034 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02400034 about?
NCT02400034 is a clinical study titled "Comparing Voiding Trials After Midurethral Sling for Stress Incontinence". Urinary incontinence is a prevalent health and quality of life concern affecting almost half of women over the age of 20. Urinary retention (abnormal holding of urine) is a concern of many surgeons who perform midurethral sling surgery. All patients after outpatient midurethral sling or vaginal prol...
What is the current status of trial NCT02400034?
This trial is currently completed. It is a NA study. The enrollment target is 112 participants. The study started on 2015-03. Estimated completion is 2016-06.
What interventions are being tested in trial NCT02400034?
The interventions under investigation include: Voiding trial (OTHER).
Who is sponsoring clinical trial NCT02400034?
This trial is sponsored by Northwell Health, which has 370 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02400034's enrollment target sits among peer trials
112 813th of 2000 higher than 1,185 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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