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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT00498888 Completed - Clinical trials for Urge Urinary Incontinence

The Long Term Outcomes of Rehabilitation and Drug Treatment for in Urgency Urinary Incontinence

UUI
Start date: June 2007
Phase: N/A
Study type: Interventional

- Urinary Urge Incontinence (UUI) is the involuntary urine loss associated with a strong sensation to void. - UUI usually associated with reduced bladder capacity. - The pathophysiology is unclear. - Pelvic floor muscle dysfunction and detrusor instability have been suggested as possible mechanisms. - Standard treatment includes anticholinergic medication and behavior modification. - The study aims to compare the long term effectiveness of 4 different approaches to the treatment of women with Urge Urinary Incontinence (UUI): 1. Pelvic Floor Rehabilitation (includes muscle training+behavioral intervention+bladder training) 2. Pelvic Floor muscle training alone 3. Bladder Training alone 4. Drug treatment with Tolterodine. - Study variables will include: impairment ratings, quality of life, and cost-effectiveness. - This study addresses three issues: 1. The long term efficacy and cost-effectiveness of the various treatment options. 2. To identify the factors involved in determining the effectiveness of drug or behavioral therapy. 3. The pathophysiology of UUI. By subdividing the rehabilitation group into 3 arms, we hope to shed light on the mechanism of dysfunction. A better response in one group will help localize the problem to pelvic floor muscles or to detrusor instability.

NCT ID: NCT00492596 Completed - Clinical trials for Urinary Incontinence, Stress

The AttenueX IntraVesical System for the Treatment of Female Stress Urinary Incontinence

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

Over 11 million women in the United States suffer from stress urinary incontinence (SUI), the involuntary leakage of urine during routine physical activities such as laughing, coughing, exercising, or sneezing. SUI affects women of all ages and can result in significant emotional distress. The purpose of this study is to evaluate a non-surgical, investigational treatment intended to reduce or eliminate urine leakage due to stress urinary incontinence.

NCT ID: NCT00490438 Recruiting - Clinical trials for Urinary Incontinence

Measurement of Vaginal Squeeze Pressure in Incontinent Patients

Start date: January 2007
Phase: N/A
Study type: Observational

The patients will be submited to a vaginal squeeze pressure measurements before and after surgeries for urinary incontinence.

NCT ID: NCT00475839 Completed - Clinical trials for Stress Urinary Incontinence

Study Comparing Tension-free Vaginal Tape With the Monarc Procedure for Stress Urinary Incontinence

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

Urinary incontinence is a major health issue in women. It is estimated to affect 30 - 40% of older women. Stress urinary incontinence, the most common form of this disease, is treated primarily with surgery. A woman's lifetime risk of surgery for SUI is 4%, with nearly 1/3 of surgery being performed for recurrences. Many different surgical procedures have been described for the treatment of SUI and there is no general agreement as to the most effective. This study compares the safety and efficacy of the tension-free vaginal tape procedure to the Monarc subfascial hammock procedure in the treatment of stress urinary incontinence.

NCT ID: NCT00475696 Completed - Clinical trials for Urinary Incontinence

Urge Incontinence Bladder Overactivity Study

Start date: November 2002
Phase: Phase 2
Study type: Interventional

Examine the efficacy and safety of duloxetine in subjects with symptoms of bladder overactivity due to pure detrusor instability or sensory urgency. Subjects in study will be permitted to escalate or de-escalate between 80 mg/day and 120 mg/day in consultation with the investigator and based on their adverse events.

NCT ID: NCT00475397 Completed - Clinical trials for Urinary Incontinence, Stress

Duloxetine Stress Urinary Incontinence Efficacy and Safety Study

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

Study F1J-MC-SBBU will examine the effect of duloxetine treatment in women with SUI. The inclusion and exclusion criteria of this Phase 3 study will ensure that all subjects have a clinical diagnosis of SUI.

NCT ID: NCT00475358 Completed - Clinical trials for Urinary Incontinence, Stress

Efficacy and Safety Stress Urinary Incontinence Study

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

Study F1J-MC-SBBT will examine the effect of duloxetine treatment in women with SUI. The inclusion and exclusion criteria of this Phase 3 study will ensure that all subjects have a clinical diagnosis of SUI.

NCT ID: NCT00472069 Completed - Clinical trials for Stress Urinary Incontinence

A New Therapeutic Strategy for Urethral Sphincter Insufficiency

Start date: April 2007
Phase: Phase 1
Study type: Interventional

Stress urinary incontinence is a frequent condition that can be caused by urethral sphincter insufficiency and results in a dramatic deterioration of the quality of life. We developed a new therapeutic strategy for stress urinary incontinence based on the implantation myofibers with their satellite cells in the urethra. The aim of this procedure is to generate functional tissue acting like a new sphincter in the urethra

NCT ID: NCT00463554 Completed - Clinical trials for Stress Urinary Incontinence

TVT-SECUR A Pilot Study for the Treatment of Stress Urinary Incontinence

Start date: April 1, 2006
Phase:
Study type: Observational

The primary objective of this study is to obtain clinical performance information on the GYNECARE TVT-SECUR* System (Tension-free Support for Incontinence) in women with stress urinary incontinence (SUI).

NCT ID: NCT00453739 Completed - Clinical trials for Stress Urinary Incontinence

TVT Worldwide Registry

Start date: February 2007
Phase: N/A
Study type: Observational

The objective of this observational study is to obtain long -term clinical and patient reported outcomes on the use of the GYNECARE family of TVT (Tension-Free Vaginal Tape) systems in women with stress urinary incontinence.