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Stress Urinary Incontinence clinical trials

View clinical trials related to Stress Urinary Incontinence.

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NCT ID: NCT00441454 Completed - Clinical trials for Stress Urinary Incontinence

Retropubic vs. Transobturator Tension-free Vaginal Tape

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

The so-called tension-free vaginal tape (TVT), first described in Sweden in 1996, has become a standard operation worldwide for the treatment of women with stress urinary incontinence. This tape is placed from the vagina behind the pubic bone and exits through the skin of the lower abdomen, just above the pubic bone. In 2001 a urologist in France proposed passing a similar tape laterally (as opposed to behind the pubic bone). This tape is passed through a window of the pelvic bones (the so-called obturator foramen), by what is called a transobturator approach. It is passed through the skin of the thigh (as opposed to the lower abdomen). The reason for this modification was to avoid injuring the bladder and, possibly, provide a more physiologic restoration of the continence mechanism. However, it is unclear whether the lateral (so-called transobturator approach) is as good as or better than the initial approach behind the pubic bone. The purpose of the present study is to compare the standard (retropubic) and the newer (transobturator) approach for the placement of a tape for treating women with stress urinary incontinence.

NCT ID: NCT00427778 Terminated - Clinical trials for Urinary Incontinence

Incontinence Ring on Stress Urinary Incontinence

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

This study aims as defining success rate of the incontinence ring in women with test proven stress urinary incontinence and determining factors associated with successful use.

NCT ID: NCT00271037 Completed - Clinical trials for Pelvic Organ Prolapse

Colpocleisis for Advanced Pelvic Organ Prolapse

Start date: July 2004
Phase: N/A
Study type: Observational

Pelvic organ prolapse occurs when the pelvic organs (e.g., the uterus or bladder) fall or slide down into the vagina. Pelvic organ prolapse can be corrected with surgery. Some types of surgery try to restore the normal anatomy and function of the vagina (i.e., reconstructive surgery). Other surgery repairs the prolapse by essentially closing the vagina (e.g., colpocleisis or colpectomy), thereby leaving a woman unable to have vaginal intercourse in the future. The use of colpocleisis has not been well-studied. The current literature is lacking sufficient studies of colpocleisis to fully understand its risks and benefits for women considering surgery for prolapse. Traditionally, colpocleisis has been restricted to elderly women thought to be poor medical risks for prolonged reconstructive surgery. This study will describe the postoperative course of women who undergo colpocleisis, with particular attention to the persistence or recurrence of urinary incontinence and patient satisfaction after the colpocleisis prolapse surgery.

NCT ID: NCT00270998 Completed - Clinical trials for Urinary Incontinence

ATLAS: Ambulatory Treatments for Leakage Associated With Stress

Start date: June 2005
Phase: Phase 3
Study type: Interventional

Stress urinary incontinence is the uncontrollable leakage of urine with physical effort or stress, such as coughing, sneezing, or exercise. Treatment for stress incontinence can be surgical or non-surgical. Different non-surgical treatments include pelvic muscle exercises and pessary use. Pelvic muscle exercises (often known as "Kegel" exercises) train and strengthen the pelvic muscles and improve incontinence. A pessary is a medical device that fits inside the vagina to give the urethra and bladder extra support and prevent or reduce urinary incontinence. Exercises and pessary use can help women with stress incontinence but it is not known which treatment is better, or if a combination of the two treatments at the same time is best. This study will determine whether pelvic muscle training and exercises, pessary use, or a combination of both exercises and pessary is most effective at improving incontinence in women. The study's primary hypothesis is that pessary use is more effective than pelvic muscle exercises after 3 months of treatment.

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: 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: 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: NCT00190905 Completed - Clinical trials for Stress Urinary Incontinence

Safety and Effectiveness Study of Duloxetine HCl in Women of Different Backgrounds With Stress Urinary Incontinence Who May Also Have Other Various Medical Conditions.

Start date: February 2004
Phase: Phase 4
Study type: Interventional

The purpose of the trial is to study the safety and effectiveness of duloxetine HCl in women of different backgrounds with stress urinary incontinence who may also have other various medical conditions.

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.