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NCT01091844 · ClinicalTrials.gov registry record · NA
Efficacy of Retrograde Fill Vs Spontaneous Fill to Assess Voiding Function
A NA study, sponsored by University of North Carolina, Chapel Hill.
- Completed
- Registry status
- NA
- Development phase
- 50
- Enrollment target
NCT01091844: Completed NA study, sponsored by University of North Carolina, Chapel Hill.
NCT01091844 is a NA study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 50 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01091844, a NA study, has completed, sponsored by University of North Carolina, Chapel Hill.
- COMPLETED
- Registry status
- NA
- Development phase
- 50 participants
- Enrollment target
Study Summary
Purpose: The purpose of this study is to determine if two different methods of performing a postoperative voiding trial are equivalent in evaluating urinary retention after gynecologic surgery. Participants: The participants in this study will be women who have undergone gynecologic surgery at UNC-Chapel Hill.
Interventions
- PROCEDURE Voiding Trial
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 50 participants |
| Start Date | 2009-12 |
| Est. Completion | 2010-08 |
| Phase | NA |
What the finished NCT01091844 record still lists
NCT01091844 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 1 intervention - of which Voiding Trial is the first listed.
NCT01091844 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01091844 about?
NCT01091844 is a clinical study titled "Efficacy of Retrograde Fill Vs Spontaneous Fill to Assess Voiding Function". Purpose: The purpose of this study is to determine if two different methods of performing a postoperative voiding trial are equivalent in evaluating urinary retention after gynecologic surgery. Participants: The participants in this study will be women who have undergone gynecologic surgery at UNC-...
What is the current status of trial NCT01091844?
This trial is currently completed. It is a NA study. The enrollment target is 50 participants. The study started on 2009-12. Estimated completion is 2010-08.
What interventions are being tested in trial NCT01091844?
The interventions under investigation include: Voiding Trial (PROCEDURE).
Who is sponsoring clinical trial NCT01091844?
This trial is sponsored by University of North Carolina, Chapel Hill, which has 1,109 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01091844's enrollment target sits among peer trials
50 1279th of 2000 higher than 622 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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