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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 is a NA study that has completed, run by Northwell Health. The registered enrollment target is 184 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02753920
The ClinicalTrials.gov registry entry for NCT02753920 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 184 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Northwell Health, which has 370 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which voiding trial is the first listed.
NCT02753920 reports 0 study locations.
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.
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