Clinical Trials Logo

Overactive Bladder clinical trials

View clinical trials related to Overactive Bladder.

Filter by:

NCT ID: NCT00290563 Completed - Clinical trials for Urinary Incontinence

Safety and Efficacy of MK0594 to Treat Overactive Bladder (0594-003)

Start date: February 21, 2006
Phase: Phase 2
Study type: Interventional

This study is designed to investigate whether a new drug may offer safe and effective treatment for patients with overactive bladder.

NCT ID: NCT00282490 Completed - Clinical trials for Urinary Incontinence

Surface Nerve Stimulation Treatment for OAB in Children

Start date: February 2006
Phase: N/A
Study type: Interventional

The purpose of this study is to perform a randomized controlled investigation of the effect of surface nerve stimulation on functional daytime incontinence in children with OAB.

NCT ID: NCT00238680 Completed - Clinical trials for Urinary Incontinence

Programmable Timer in the Bladder Rehabilitation Treatment of OAB

Start date: March 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of bladder rehabilitation in a non-selected group of children with idiopathic overactive bladder and to clarify whether the effect of the treatment can be increased by addition of a programmable timer

NCT ID: NCT00231491 Completed - Overactive Bladder Clinical Trials

Efficacy and Safety of Botulinum Toxin A for the Treatment of Refractory Overactive Bladder.

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

Overactive bladder induce urgency, urge incontinence, nocturia and pollakiuria. This condition is often resistant to anticholinergic drugs used as a first line treatment for this purpose. Moreover muscarinic side effects (constipation, mouth dryness) often limits the use of those treatments. This study is designed to evaluate the efficacy and safety of botulinum toxin A injected into the detrusor muscle to control symptoms and improve quality of life for patients resistant or intolerant to anticholinergic drugs.

NCT ID: NCT00224146 Completed - Quality of Life Clinical Trials

Transdermal (TDS) Oxybutynin (Oxytrol(r)) in Overactive Bladder

MATRIX
Start date: May 2004
Phase: Phase 4
Study type: Interventional

This study evaluates changes in health related quality of life outcomes in patients using Oxytrol(r)

NCT ID: NCT00220389 Completed - Overactive Bladder Clinical Trials

Two Phase Extension Trial of SP668 to Investigate the Safety and Tolerability of Sustained Release Fesoterodine in Subjects With Overactive Bladder: a Double-Blind Phase Followed by an Open-Label Extension Phase

Start date: June 2003
Phase: Phase 2
Study type: Interventional

This extension trial of SP668 consists of two phases: double-blind treatment and open-label extension. The trial provides subjects the option of long-term treatment with sustained release (SR) fesoterodine (SPM 907) and to assess long-term subject safety, tolerability and efficacy. Double-Blind: Subjects remained on either fesoterodine 4mg, 8mg or 12mg depending on their dose assignment in SP668. Previous SP668 placebo subjects received fesoterodine 4mg. Open-Label: Subjects received fesoterodine 8mg with a one time option to reduce the dose to 4mg and a one time option to increase again to 8mg. The primary variables focus on long-term safety and tolerability and include the observation and assessment of adverse events, residual urinary volumes, laboratory parameters, changes in ECG, physical and urological examinations and subject's assessment of treatment tolerance. Secondary efficacy variables include various parameters derived from micturition diaries, count of subjects and their dose choice throughout the trial and subject's assessment of treatment efficacy.

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.