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Urinary Bladder, Overactive clinical trials

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NCT ID: NCT01004315 Completed - Overactive Bladder Clinical Trials

A Confirmatory Study of KUC-7483 in Patients With Overactive Bladder

Start date: n/a
Phase: Phase 3
Study type: Interventional

To evaluate the efficacy and the safety of KUC-7483 in overactive bladder patients.

NCT ID: NCT00985387 Completed - Overactive Bladder Clinical Trials

Evaluation of Adherence to Solifenacin Treatment in Overactive Bladder Patients

Start date: August 2009
Phase: N/A
Study type: Observational

The purpose of the study is to assess patient's persistency in maintaining solifenacin treatment for overactive bladder.

NCT ID: NCT00979472 Completed - Overactive Bladder Clinical Trials

Solifenacin Flexible Dosing Study in Frequent Micturition Patients With and Without Urgency

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

The purpose of the study is to compare the effect of solifenacin succinate between frequent micturition patients with urgency and those without urgency.

NCT ID: NCT00971646 Completed - Osteoporosis Clinical Trials

Cohort Study: Perceptual Urge Sensation

Start date: June 2010
Phase:
Study type: Observational

Over the past few years it has become clear that our understanding of bladder physiology is inadequate to explain urge incontinence. This has forced us to re-evaluate what we know and do not know about bladder function and dysfunction. This has led to the identification and study of novel systems within the bladder that may contribute to abnormal sensations. The investigators now suspect that the organic changes occurring in the bladder are not the whole story. For one group of patients with pathological urge there is growing evidence suggesting that there may be a strong psychological component. The idea now being put forward is that normal afferent peripheral information is perceived as abnormal and excessive, resulting in an increased desire to go to the bathroom: 'perceptual urge'. It is important to identify this group of patients since it will direct their treatment towards more cognitive approaches. Also, if such a psychological aetiology can be eliminated it would lead to a more focused and effective management of peripheral pathology with surgery or pharmacology.

NCT ID: NCT00966004 Completed - Clinical trials for Urinary Bladder, Overactive

A Study to Evaluate Safety and Efficacy of YM178 in Patients With Overactive Bladder

Start date: July 2009
Phase: Phase 3
Study type: Interventional

The purpose of the study is to evaluate the effect of YM178 in patients with overactive bladder for 12-week administration.

NCT ID: NCT00943904 Completed - Overactive Bladder Clinical Trials

Comparison of Motor and Sensory Response With Interstim Stimulation

Start date: July 2009
Phase: N/A
Study type: Interventional

Sacral nerve stimulation (SNS) implantation is a minimally invasive procedure which has current FDA approval for urinary urge incontinence, urgency-frequency syndrome and non-obstructive urinary retention, and has been available in the United States since 1997. The SNS delivers non-painful, mild electrical pulses to the sacral nerves to modulate the reflexes that influence the bladder, sphincter, and pelvic floor to improve or restore normal voiding function. While SNS has been shown to have efficacy for the aforementioned conditions, the exact mechanism of action is unknown, but it is believed to work primarily through the somatic afferent system in promoting inhibitory reflex pathways to facilitate urine storage. The degree of stimulation is thought to be at a level that only evokes a sensory and not a motor response; however this has not been tested.

NCT ID: NCT00943735 Completed - Overactive Bladder Clinical Trials

This Is An Open-Label Study To Evaluate Fesoterodine Plus "Your Way" Patient Support Plan In Patients With Symptoms Of Overactive Bladder

Start date: July 2009
Phase:
Study type: Observational

The primary objective of the study is to assess the level of medication adherence observed among subjects receiving a specific combination of education and support materials (YourWay plan) along with a prescription for fesoterodine.

NCT ID: NCT00932022 Completed - Obesity Clinical Trials

Trospium Chloride XR in Obese Female Patients With Overactive Bladder

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

This study evaluated the effectiveness of trospium chloride extended release (XR) in obese female patients with overactive bladder (OAB). Patients received either placebo and trospium chloride XR or placebo only. The study assessed the change from baseline in urinary frequency, urgency, and incontinence for trospium chloride XR versus a placebo-pill. The study was 14 weeks in duration.

NCT ID: NCT00928395 Completed - Clinical trials for Urinary Bladder, Overactive

Modified Extension Study to the SUmiT Trial: Evaluation of Long Term Therapy With Percutaneous Tibial Nerve Stimulation (PTNS) for Overactive Bladder Symptoms

STEP
Start date: January 2009
Phase: Phase 4
Study type: Interventional

This is a modified extension study to the SUmiT protocol UPC082008 (NCT00534521) to observe and evaluate long term therapy with PTNS on overactive bladder symptoms. Subjects must have completed the 12 weekly treatments of the original protocol, the 13 week follow up assessment, be randomized to the PTNS arm, and be considered a positive responder with moderate or marked improvement in the SUmiT Trial to be enrolled in this study. All consenting responders will continue with active PTNS therapy at an initially prescribed protocol for approximately 3 months followed by individualized symptom-based frequency of visits as determined by the subject along with their treating clinician, for up to a total of 33 months post initial 12-week therapy for a total of 3 years.

NCT ID: NCT00928070 Completed - Overactive Bladder Clinical Trials

A Study Of Efficacy And Safety Of Fesoterodine In Vulnerable Elderly Subjects With Overactive Bladder

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

This study is designed to assess the efficacy and safety of a flexible dose regimen of fesoterodine on urgency urinary incontinence (UUI) episodes in vulnerable elderly subjects with overactive bladder (OAB).