CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 79 enrolled
Drug / intervention
Voiding Trialgenetic
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00392210
NCT00392210N/ACompleted
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Assessment of Two Postoperative Techniques Used to Predict Voiding Efficiency After Gynecologic Surgery

University of Rochester·interventional·Posted Oct 25, 2006·Updated Apr 27, 2017

In Brief

A clinical study evaluating Voiding Trial for Urinary Incontinence. Completed, enrolled 79 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsUrinary Incontinence
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 25, 2006
Enrollment StartOct 1, 2006
Primary CompletionOct 1, 2009
TodayJul 2, 2026
Enrollment to primary: 3 yearsPosted 19.7 years ago

Interventions

Voiding Trialgenetic

Post-void residual and uroflow study will be done twice