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Urinary Bladder, Overactive clinical trials

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NCT ID: NCT01099345 Terminated - Bladder Function Clinical Trials

A Pilot Trial in a Sleep Laboratory Setting to Observe Night Time Bladder Function of Subjects With Overactive Bladder (OAB)

Start date: July 2010
Phase: N/A
Study type: Observational

This is an observational, pilot, non-treatment study to evaluate and develop clinical variables for distinguishing female OAB subjects that have detrusor overactivity positive (DO+) nocturia from female OAB subjects that have detrusor overactivity negative (DO-) nocturia utilizing a sleep laboratory setting.

NCT ID: NCT01091519 Terminated - Clinical trials for Urinary Bladder, Overactive

Non-Interventional Study To Investigate Whether Information Provided To Patients Influences Their Satisfaction With Toviaz Therapy

Start date: December 2010
Phase: N/A
Study type: Observational

Collect information on treatment with Toviaz (fesoterodine) under ordinary prescribing conditions, and to investigate whether additional educational information affects satisfaction with treatment as perceived by the patient.

NCT ID: NCT01023269 Terminated - Clinical trials for Urinary Incontinence

Efficacy Study of Pudendal Neuromodulation for the Treatment of Neurogenic Overactive Bladder

ACCEPTANCE
Start date: December 2009
Phase: N/A
Study type: Interventional

The study is designed to demonstrate that treatment with low level stimulation of the bladder muscles reduces symptoms of urinary incontinence in comparison with no stimulation.

NCT ID: NCT01003249 Terminated - Constipation Clinical Trials

Dysfunctional Voiding and Lower Urinary Tract Symptoms With Baclofen

Start date: September 2009
Phase: Phase 4
Study type: Interventional

Dysfunctional voiding is often associated with constipation. The association of constipation with urologic pathologic processes has previously been described since the 1950's, but it was only over the past decade that clinicians have paid more attention to this relationship and recognized it existence with the term dysfunctional elimination syndrome (DES). This term is used to reflect the broad spectrum of functional disturbances that may affect the urinary tract including that of functional bowl disturbances and can be classified as follows: - Functional disorder of filling: overactive bladder, over distention of bladder or insensate bladder, which may be associated with fecal impaction or rectal distention with infrequent bowel movements - Functional disorder of emptying: over-recruitment of pelvic floor activity during voiding causing interrupted and/or incomplete emptying also associated with defecation difficulties due to non- relaxation of the puborectalis muscle, dyssynergic defecation or pain with defecation Several different therapeutic options have been used for patients with dysfunctional voiding mainly to decrease bladder outlet obstruction. These treatments including, alpha adrenergic antagonists, and botulinum toxin are less than optimum. One possible explanation for these drug failures includes the inability of these medications to relax the striated muscles of the pelvic floor necessary for voiding. To date there has been no data to evaluate the role of baclofen on the striated muscle of the external anal sphincter, essential in the defecation process.

NCT ID: NCT00871975 Terminated - Overactive Bladder Clinical Trials

Diagnostic Utility of Tetra-NIRS in Conjunction With Urodynamic Studies

Start date: April 2009
Phase: Phase 4
Study type: Interventional

The purpose of this evaluation is to validate the previous clinical study results using the Tetra-NIRS as compared to the conventional UDS in the voiding procedure. The experiment will use a commercially available Tetra-NIRS device. The hypothesis is that the commercially available Tetra-NIRS device, in the clinical environment, provides data to enhance the analysis using the standard urodynamics equipment (stand-alone Urodynamic procedure).

NCT ID: NCT00852696 Terminated - Overactive Bladder Clinical Trials

Over Active Bladder Patients Having Sling Surgery

Start date: February 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether treatment with anti-muscarinic medications following sub-urethral sling procedures improves overall subjective and objective outcomes in women with mixed incontinence with primary stress symptoms.

NCT ID: NCT00821184 Terminated - Overactive Bladder Clinical Trials

Behavioral Modification and Vesicare Versus Vesicare Alone for Urge Incontinence in Patients With Overactive Bladder

Start date: September 2006
Phase: Phase 3
Study type: Interventional

This study will help determine if behavior modification performed in conjunction with oral Vesicare anticholinergic therapy is more effective for treating overactive bladder symptoms than oral Vesicare anticholinergic therapy alone.

NCT ID: NCT00805779 Terminated - Clinical trials for Urinary Bladder, Overactive

Pulsed Electromagnetic Stimulation for Treatment of Overactive Bladder

Start date: December 2008
Phase: N/A
Study type: Interventional

To assess the initial safety and clinical feasibility of neuromodulation therapy in treating patients with documented overactive bladder. The specific aim is improved urinary frequency and urgency after 12 weeks of treatment

NCT ID: NCT00780832 Terminated - Overactive Bladder Clinical Trials

Comparison of Caffeine Reduction and Anticholinergic Medications for Treatment of Overactive Bladder

Start date: May 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the effects of caffeine reduction/elimination on urinary symptoms in women with overactive bladders and compare this therapeutic approach to anticholinergic therapy. We hope to show a reduction in symptoms with caffeine reduction and determine how effective caffeine reduction is compared to medication. If caffeine reduction is shown to be beneficial, women may be encouraged to use this strategy before resorting to medications.

NCT ID: NCT00759577 Terminated - Overactive Bladder Clinical Trials

Feasibility of "At-home" Titration of Solifenacin

Start date: September 2008
Phase: Phase 4
Study type: Interventional

This is an open-label single center trial to study improvements in symptom bother and quality of life in overactive bladder patients self titrating solifenacin 5mg and 10 mg. The study is designed to reflect real world conditions in typical male and female OAB patients presenting for treatment.