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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 is a NA study that has completed, run by University of North Carolina, Chapel Hill. The registered enrollment target is 50 participants.
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 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01091844
The ClinicalTrials.gov registry entry for NCT01091844 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 50 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of North Carolina, Chapel Hill, which has 1,109 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Voiding Trial is the first listed.
NCT01091844 reports 0 study locations.
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.
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