UNGF Assessment in Patients With Detrusor Overactivity Undergoing Sacral Neuromodulation
Completed
Conditions studied: Detrusor Overactivity
In brief
The purpose of this study is to find a noninvasive test to help physicians diagnose detrusor overactivity (DO), to use this urine test to help diagnose bladder problems, determine if treatments are working, and determine if patients are good candidates for interventions like sacral neuromodulation/Interstim Therapy.
Key facts
- Study ID
- NCT01850706
- Run by
- Northwell Health
- People needed
- 50
- Starts
- 2011-08-01
- Expected to finish
- 2016-03-01
- Last updated by the study team
- 2016-10-26
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- for controls: age greater than or equal to 18; female gender, ability to provide informed consent and complete study requirements; subject has to be without urinary symptoms
- for cases: age greater than or equal to 18; female gender; ability to provide informed consent and complete study requirements; the subject should have symptoms of detrusor overactivity, including urinary frequency, urgency, or urge incontinence, for greater than or equal to 3 months; urodynamic diagnosis of detrusor overactivity; failed treatment with behavioral modification and anticholinergic medication
You may not qualify if…
- active urinary tract infection; currently undergoing hemodialysis or has severe renal impairment; bladder tumors; uncontrolled diabetes mellitus; post void residual greater than 100ml; history of use of anticholinergic treatment within past 21 days; history of urinary tract operation within 6 months prior to screening; heart failure; uncontrolled hypertension; severe neurological disease; history of botox usage within 1 year
Where it is running
- North Shore University Hospital — Manhasset, New York, United States
Full record on ClinicalTrials.gov
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