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Overactive Bladder clinical trials

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NCT ID: NCT00212732 Completed - Overactive Bladder Clinical Trials

Controlled Study of ONO-8025 (KRP-197) in Patients With Overactive Bladder in Japan

Start date: October 2003
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of ONO-8025 (KRP-197) in patients with overactive bladder.

NCT ID: NCT00212706 Completed - Overactive Bladder Clinical Trials

Controlled Study of ONO-8025 (KRP-197) in Patients With Overactive Bladder in Japan

Start date: October 2001
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of ONO-8025 (KRP-197) in patients with overactive bladder.

NCT ID: NCT00189800 Completed - Overactive Bladder Clinical Trials

A Study of Solifenacin Succinate Compared to Tolterodine in Patients With Overactive Bladder

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

The purpose of this study is to ascertain the clinical results of solifenacin succinate of PIII study conducted in the original country using Korean patients with an overactive bladder.

NCT ID: NCT00174798 Completed - Overactive Bladder Clinical Trials

MILADY: A Randomized, Placebo-controlled Safety and Efficacy Trial of SSR240600C in Treatment of Overactive Bladder or Urge Urinary Incontinence.

Start date: May 2005
Phase: Phase 2
Study type: Interventional

To evaluate the safety and efficacy of SSR240600C versus placebo on clinical and cystometric parameters in patients with OAB and UUI.

NCT ID: NCT00171184 Completed - Overactive Bladder Clinical Trials

Efficacy, Safety, and Tolerability of Darifenacin in Patients Aged > 65 Years With Overactive Bladder

Start date: April 2005
Phase: Phase 4
Study type: Interventional

The objective of this study is to assess the efficacy, safety and tolerability of 12-weeks treatment with darifenacin in patients aged >Ý 65 years with OAB.

NCT ID: NCT00168454 Completed - Clinical trials for Urinary Incontinence

A Research Study for Patients With Overactive Bladder

Start date: July 2005
Phase: Phase 2
Study type: Interventional

The purpose of this study is to investigate whether injections of botulinum toxin Type A into the bladder are safe and effective in treating overactive bladder.

NCT ID: NCT00138723 Completed - Overactive Bladder Clinical Trials

Trial to Investigate the Efficacy, Tolerability and Safety of Fesoterodine Sustained Release in Subjects With Overactive Bladder Syndrome

Start date: October 2003
Phase: Phase 3
Study type: Interventional

This Phase 3 trial will investigate the efficacy, tolerability and safety of fesoterodine fumarate (SR) (fesoterodine; SPM 907) in adult male and female subjects with overactive bladder syndrome. The trial is a randomized, double-blind placebo controlled multicenter trial. The trial consisted of a 2 week Run-In period, 12 week double-blind Treatment period and 2 week Safety Follow-Up period. Subjects were randomized to one of 3 treatment arms receiving either fesoterodine fumarate 4mg, fesoterodine fumarate 8mg, or placebo during the double-blind Treatment period. Two primary efficacy variables will be assessed for submission in the United States: change in the average number of micturitions (frequency) per 24 hours and the change in the average number of urge incontinence episodes per 24 hours. For the submissions in the European Union, the first primary variable will be the change in the average number of micturitions (frequency) per 24 hours and the co-primary variable is the treatment response, based on a treatment benefit scale. All continuous variables will be measured as changes from baseline to value after 12 weeks of treatment. The following safety variables were observed and assessed: adverse events, change in residual urinary volume (mL), change in laboratory parameters, change in vital signs, change in electrocardiogram (ECG), change in physical examination and change in urological/urogynecological examination.

NCT ID: NCT00131573 Completed - Overactive Bladder Clinical Trials

An Implantable Microstimulator for the Chronic Treatment of Urinary Urgency-Frequency Syndrome

Start date: May 2004
Phase: Phase 3
Study type: Interventional

The goal of this study is to investigate the safety and effectiveness of a new implanted device designed to treat Urinary Urgency-Frequency Syndrome.