Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT00392210 · ClinicalTrials.gov registry record · NA
Assessment of Two Postoperative Techniques Used to Predict Voiding Efficiency After Gynecologic Surgery
A NA study, sponsored by University of Rochester.
- Completed
- Registry status
- NA
- Development phase
- 79
- Enrollment target
NCT00392210 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 79 participants.
The verdict
NCT00392210, a NA study, has completed, sponsored by University of Rochester.
- COMPLETED
- Registry status
- NA
- Development phase
- 79 participants
- Enrollment target
Study Summary
After gynecologic surgery, it may be difficult to void (urinate). This problem is usually short-term with normal function returning within a few days to a few weeks. For this reason, patients may require drainage of their bladder with a catheter immediately after surgery. Currently in our office, we use two different tests to see how well you are able to urinate and how quickly the catheter can be removed. The purpose of this study is to see which voiding test is better after gynecologic surgery.
Interventions
- GENETIC Voiding Trial
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 79 participants |
| Start Date | 2006-10 |
| Est. Completion | 2009-10 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00392210
The ClinicalTrials.gov registry entry for NCT00392210 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 79 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Rochester, which has 636 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.
NCT00392210 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00392210 about?
NCT00392210 is a clinical study titled "Assessment of Two Postoperative Techniques Used to Predict Voiding Efficiency After Gynecologic Surgery". After gynecologic surgery, it may be difficult to void (urinate). This problem is usually short-term with normal function returning within a few days to a few weeks. For this reason, patients may require drainage of their bladder with a catheter immediately after surgery. Currently in our office, we...
What is the current status of trial NCT00392210?
This trial is currently completed. It is a NA study. The enrollment target is 79 participants. The study started on 2006-10. Estimated completion is 2009-10.
What interventions are being tested in trial NCT00392210?
The interventions under investigation include: Voiding Trial (GENETIC).
Who is sponsoring clinical trial NCT00392210?
This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
Explore more on PlainTrial
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.