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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT00392210 Completed - Clinical trials for Urinary Incontinence

Assessment of Two Postoperative Techniques Used to Predict Voiding Efficiency After Gynecologic Surgery

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

After gynecologic surgery, it may be difficult to void (urinate). This problem is usually short-term with normal function returning within a few days to a few weeks. For this reason, patients may require drainage of their bladder with a catheter immediately after surgery. Currently in our office, we use two different tests to see how well you are able to urinate and how quickly the catheter can be removed. The purpose of this study is to see which voiding test is better after gynecologic surgery.

NCT ID: NCT00378664 Completed - Clinical trials for Urinary Incontinence

Lumbar to Sacral Ventral Nerve Re-Routing

Start date: September 2006
Phase: Phase 2
Study type: Interventional

To assess the level of improvement in voiding function after lumbar to sacral ventral nerve re-routing procedure in Spinal Cord Injury and spina bifida patients

NCT ID: NCT00376441 Completed - Surgery Clinical Trials

Evaluate Women After Vaginal Surgery for Urinary Symptoms and Sexual Function

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

Assess the outcomes of vaginal surgeries and its impact on sexual function and urinary symptoms.

NCT ID: NCT00345332 Completed - Clinical trials for Urinary Incontinence

A Multi-Center Trial of Botox for Severe Urge Urinary Incontinence

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

The purpose of the 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: NCT00337558 Completed - Clinical trials for Urinary Incontinence

A Study of Solifenacin With Bladder Training Versus Solifenacin Alone in Patients With Overactive Bladder (SOLAR)

SOLAR
Start date: May 2006
Phase: Phase 4
Study type: Interventional

This study will look at a drug for OAB (solifenacin) in combination with a non drug treatment (bladder training) compared to the drug on its own. The study will compare the symptoms of OAB by assessing patient diaries and other patient reported outcomes.

NCT ID: NCT00333112 Completed - Clinical trials for Urinary Incontinence

A Study to Evaluate Solifenacin Succinate in Combination With Tamsulosin for the Treatment of Residual Overactive Bladder Symptoms (OAB) in Men.

VICTOR
Start date: May 2006
Phase: Phase 4
Study type: Interventional

A study to evaluate solifenacin succinate in combination with tamsulosin for the treatment of residual OAB symptoms in men.

NCT ID: NCT00333073 Completed - Clinical trials for Urinary Incontinence

Effectiveness and Safety of Bulkamid® as Bulking Agent for the Treatment of Female Urinary Incontinence

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

To assess effectiveness of Bulkamid® injection in females suffering from stress or mixed (stress and urge) urinary incontinence after 12 months follow up period

NCT ID: NCT00325039 Completed - Clinical trials for Urinary Incontinence

TOMUS-Trial Of Mid-Urethral Slings

TOMUS
Start date: April 2006
Phase: Phase 4
Study type: Interventional

The primary aim of this clinical trial is to compare treatment success for two minimally invasive surgical procedures to treat stress urinary incontinence in women. These procedures are called mid-urethral slings. The secondary aims of the trial are to compare other outcomes for the two surgical procedures, including quality of life, sexual function, satisfaction with treatment outcomes, complications, and the need for other treatments(s) after surgery. Follow-up will be a minimum of two years.

NCT ID: NCT00323245 Completed - Clinical trials for Urinary Incontinence

Regaining Bladder Control in Postmenopausal Women With Osteoporosis

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

Conservative management for urinary incontinence has been shown to improve bladder control. We are conducting a study of the effectiveness of conservative management for urinary incontinence in women who also have osteoporosis. We hope to find that treatment for incontinence improves bladder control and thereby allows women to be more active and reduces their risk of falling and breaking bones.

NCT ID: NCT00321477 Completed - Overactive Bladder Clinical Trials

A Study Of GW679769 Compared To Placebo In Women With Overactive Bladder

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

This is a Phase IIa study to evaluate the efficacy, safety and tolerability of GW679769 vs placebo on symptoms of urgency with urge incontinence, frequency and nocturia associated with overactive bladder in women.