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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT00190814 Completed - Clinical trials for Urinary Incontinence, Stress

Effectiveness and Safety of Duloxetine in Women Experiencing Urinary Leakage Due to Physical Stress and Urge.

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

The purpose of the study is to evaluate the effectiveness of duloxetine in reducing urinary incontinence(leakage of urine)occurrences in women due to physical stress and leakage that occurs during a strong need(urge) to urinate.

NCT ID: NCT00190645 Completed - Clinical trials for Stress Urinary Incontinence

To Evaluate the Safety of Duloxetine in Patients With Stress Urinary Incontinence

Start date: February 2001
Phase: Phase 3
Study type: Interventional

The patients are being followed in this study to determine the safety of taking the medication Duloxetine for a long period of time. The patients participating in this study suffer from Stress Urinary Incontinence.

NCT ID: NCT00190632 Completed - Clinical trials for Stress Urinary Incontinence

To Evaluate the Safety in Patients Taking Duloxetine for Stress Urinary Incontinence

Start date: March 2001
Phase: Phase 3
Study type: Interventional

This is an on-going study to evaluate the long-term safety and maintenance of effect of duloxetine in patients suffering with stress urinary incontinence.

NCT ID: NCT00190606 Completed - Clinical trials for Urinary Stress Incontinence

Efficacy and Safety of Duloxetine, Placebo and Pelvic Floor Muscle Training in Subjects With Stress Urinary Incontinence

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

The study is a comparison of the efficacy and safety of duloxetine and pelvic floor muscle training with that of placebo in patients with moderate to severe stress urinary incontinence

NCT ID: NCT00178334 Completed - Clinical trials for Urinary Incontinence

Screening for Urinary Incontinence by Primary Care Providers

Start date: March 2006
Phase: N/A
Study type: Observational

The purpose of this study is to: - Assess the rate of screening for urinary incontinence (UI) in women by their primary care providers - Identify the type of screening used by primary care providers - Identify barriers to screening for UI - Identify differences in screening rates between specialties - Assess whether primary care providers view UI as a serious medical problem - Assess the comfort level of primary care providers in the diagnosis and treatment of UI - Identify primary care providers' preferred mode of learning more about UI

NCT ID: NCT00178191 Completed - Clinical trials for Urinary Incontinence

Randomized Trial for Botox Urinary Incontinence

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

The purpose of this study is to determine how effective Botox is in reducing the amount of urine leaked and which dose of Botox is more effective and safe in those who have urinary urge incontinence.

NCT ID: NCT00177541 Completed - Clinical trials for Urge Urinary Incontinence

Further Enhancing Non-pharmacologic Therapy for Incontinence

Start date: February 2004
Phase: N/A
Study type: Interventional

To determine the mechanisms mediating the therapeutic efficacy of pelvic floor muscle exercises and biofeedback for urge urinary incontinence, as well as the characteristics of patients most likely to respond. By identifying the key components of this treatment, we hope to simplify it and make it more easily applicable, more effective, less expensive, and thus more useful for people with urge incontinence in the future.

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: 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: NCT00164138 Completed - Cystic Fibrosis Clinical Trials

Prevalence and Treatment of Urinary Incontinence in Women With Cystic Fibrosis and Chronic Obstructive Pulmonary Disease

Start date: December 2001
Phase: N/A
Study type: Interventional

Women with chronic lung disease characterised by chronic cough report urinary incontinence. Recently there have been reports of increased urinary incontinence in girls and women with cystic fibrosis. While coughing is a known risk factor for stress incontinence, other risk factors and causes are poorly understood in this population. Treatment of incontinence for patients with chronic lung disease is also poorly addressed, adding to the burden of disease for women with chronic lung disease, carers and the health system. This project will estimate the prevalence of women with CF and COPD compared to healthy age matched controls and will evaluate the effect of a specific treatment and management program for these patients. The results will be disseminated to respiratory health professionals. We hypothesise that women with chronic cough will have a higher incidence of urinary incontinence than healthy controls and that a specific treatment program will result in alleviation of the problems and improved quality of life.