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NCT02753920 · ClinicalTrials.gov registry record · NA
Comparing Force of Stream to Retrograde Fill Voiding Trial After Vaginal Apex Suspension
A NA study, sponsored by Northwell Health.
- Completed
- Registry status
- NA
- Development phase
- 184
- Enrollment target
NCT02753920: Completed NA study, sponsored by Northwell Health.
NCT02753920 is a NA study that has completed, run by Northwell Health. The registered enrollment target is 184 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02753920, a NA study, has completed, sponsored by Northwell Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 184 participants
- Enrollment target
Study Summary
Voiding difficulties are common after prolapse and incontinence surgeries. All patients after vaginal prolapse surgery must complete a voiding trial if they are to be discharged home without a catheter. Accepted protocols for voiding trials after prolapse and incontinence surgeries do not exist. The purpose of this study is to compare two different types of postoperative voiding trials to determine which leads to less postoperative issues, such as urinary retention requiring catheterization. You are being asked to participate because you are having a vaginal apex suspension surgery.
Interventions
- OTHER voiding trial
- DEVICE Foley catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 184 participants |
| Start Date | 2016-03 |
| Est. Completion | 2018-07 |
| Phase | NA |
What the finished NCT02753920 record still lists
NCT02753920 is an interventional study that assigns participants to a tested intervention. The registered 184 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 (87% lower).
The record links to 0 conditions, and to 2 interventions - of which voiding trial is the first listed.
NCT02753920 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02753920 about?
NCT02753920 is a clinical study titled "Comparing Force of Stream to Retrograde Fill Voiding Trial After Vaginal Apex Suspension". Voiding difficulties are common after prolapse and incontinence surgeries. All patients after vaginal prolapse surgery must complete a voiding trial if they are to be discharged home without a catheter. Accepted protocols for voiding trials after prolapse and incontinence surgeries do not exist. The...
What is the current status of trial NCT02753920?
This trial is currently completed. It is a NA study. The enrollment target is 184 participants. The study started on 2016-03. Estimated completion is 2018-07.
What interventions are being tested in trial NCT02753920?
The interventions under investigation include: voiding trial (OTHER), Foley catheter (DEVICE).
Who is sponsoring clinical trial NCT02753920?
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 NCT02753920's enrollment target sits among peer trials
184 581st of 2000 higher than 1,417 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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