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Urinary Incontinence, Stress clinical trials

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NCT ID: NCT00270738 Completed - Clinical trials for Female Urinary Incontinence

Treatment for Female Stress Urinary Incontinence

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

Urinary incontinence (UI) is the complaint of any involuntary leakage of urine. Stress urinary incontinence (SUI) is the complaint of involuntary leakage on effort or exertion, or on sneezing or coughing. The prevalence of female UI is greater than that of male, and the commonest type is SUI. UI has significant impact on the quality of life including physical, mental and social issues. SUI may also lead to withdraw from regular physical exercise and fitness activities that important in the prevention of osteoporosis, coronary heart disease, and so on. The cause of SUI is related to the impairment of pelvic floor muscles (PFM). So far, the effects of intensive pelvic floor muscle training for female SUI were proved in many randomized controlled trials. However, training of accurate contraction of PFM depends on vaginal palpation. The willingness to seek for medical help may be reduced due to being embarrassed with vaginal palpation. Sapsford proposed a concept to treat SUI via transversus abdominis (TrA) that does not need to palpate the vagina. Maybe the new intervention can promote the willingness to seek medical help. However, to date there is no randomized controlled trial comparing the effect of indirect training of the PFM via TrA with either untreated control or other intervention. Therefore, there are two purposes in this study, to compare the effect of indirect training of PFM via TrA with control group and to compare the effect of indirect training of PFM via TrA with PFMT for female SUI.

NCT ID: NCT00247286 Terminated - Clinical trials for Urinary Incontinence, Stress

Weighted Vaginal Cones Versus Biofeedback in the Treatment of Urodynamic Stress Incontinence: a Randomized Trial.

Start date: September 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the objective (urodynamic) cure rates and effect on patient quality of life after six months of treatment for two different nonsurgical management options for genuine stress urinary incontinence in females: weighted vaginal cones and formal supervised pelvic floor physiotherapy with biofeedback. Hypothesis: Assuming a minimum of six months of treatment, weighted vaginal cones are as effective as a formal supervised program of pelvic floor physiotherapy with biofeedback for the treatment of uncomplicated genuine stress urinary incontinence in females.

NCT ID: NCT00244296 Completed - Clinical trials for Urinary Incontinence, Stress

To Determine How Effective Duloxetine is in Treating Women 65 Years and Older With Symptoms of Stress Urinary Incontinence, or With a Combination of Stress Urinary Incontinence and Urge Urinary Incontinence Symptoms

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

The purpose of this study is to determine how effective duloxetine is in treating women who are 65 years of age or older with symptoms of stress urinary incontinence, or with a combination of stress urinary incontinence and urge urinary incontinence symptoms.

NCT ID: NCT00234754 Completed - Clinical trials for Stress Urinary Incontinence

Trans-Obturator Tape Versus Trans-Vaginal Tape for Stress Urinary Incontinence in Women

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

Stress urinary incontinence (SUI) is a health concern for many women. The transvaginal tape (TVT) surgery has become a common procedure to address the problem. Another surgery is now available, trans-obturator tape (TOT). The investigators will compare these 2 approaches to dealing with SUI and follow the women for 1 year. Women will also be followed at 5 years after surgery.

NCT ID: NCT00223106 Completed - Clinical trials for Urinary Incontinence, Stress

Treatment for Stress and Mixed Urinary Incontinence and Vaginal Vault Prolapse

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

The primary objective of this study is to further evaluate the safety and effectiveness of the use of a sling device in women for stress and mixed urinary incontinence as well as vaginal vault prolapse.

NCT ID: NCT00222248 Completed - Clinical trials for Stress Urinary Incontinence

Pelvic Floor Muscle Training for Incontinence in Older Women.

Start date: March 3, 2003
Phase: N/A
Study type: Interventional

To determine the effect of pelvic floor muscle training in women aged 70 years and over, who have proven stress urinary incontinence. The hypotheses to be tested are: 1. That pelvic floor muscle training is effective in relief of symptoms of stress urinary incontinence as measured by a greater reduction in the number of episodes of incontinence, quantity of urine lost and improvement of quality of life. 2. That women who undertake pelvic floor muscle training will show greater improvement of pelvic floor muscle function than women who have behavioural (bladder) training, as measured by real time transabdominal ultrasound.

NCT ID: NCT00197314 Completed - Clinical trials for Urinary Stress Incontinence (SI)

Effectiveness of Circular Muscle Exercise (Paula Method) Versus Kegel Exercise for Urinary Stress Incontinence

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

This is a randomized controlled trial comparing two methods of exercise for the treatment of stress incontinence ( loss of urine after physical exertion) in women. We are comparing the Paula method of circular muscle exercise, in which circular muscles controlling sphincters of the body (such as the eyes, mouth and rectum) are exercised, with pelvic floor training (Kegel exercises) in women in the community. The study hypothesis is that the effectiveness of circular muscle exercises is equivalent to pelvic floor training among women with this disorder.

NCT ID: NCT00196521 Completed - Clinical trials for Stress Urinary Incontinence

A Clinical Evaluation of the Tension-Free Vaginal Tape Obturator System For Treatment of Stress Urinary Incontinence (Urinary Leakage)

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

Stress urinary incontinence affects nearly 30 million women worldwide and the main goal of surgical treatment is to stop urinary incontinence (urinary leakage) that occurs with physical activity, coughing, sneezing, etc.Patients in the study will have an operation to improve urinary incontinence symptoms. This will involve inserting a mesh sling to help support the urethra (tube leading into your bladder). During the operation, the study doctor will use tension-free vaginal obturator system. The study will include women diagnosed with Stress Urinary Incontinence who have completed their families.

NCT ID: NCT00191204 Completed - Clinical trials for Urinary Incontinence Stress

Open Label Phase III Duloxetine Study for Stress Urinary Incontinence

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

The purpose of this study is to monitor the long term safety of duloxetine in the treatment of stress urinary incontinence.

NCT ID: NCT00191087 Completed - Clinical trials for Urinary Incontinence, Stress

Duloxetine in the Treatment of Stress Urinary Incontinence.

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

The purpose of this study is to monitor the long term safety of duloxetine in the treatment of stress urinary incontinence.