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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT00565838 Completed - Clinical trials for Stress Urinary Incontinence

Quality-of-Life Outcomes After Autologous Fascial Sling and TVT: a Prospective Randomized Trial

Start date: January 2001
Phase: N/A
Study type: Observational

The objective of the study was to evaluate the impact AFS and TVT procedures on quality-of-life in incontinent women.

NCT ID: NCT00564226 Completed - Overactive Bladder Clinical Trials

SSR240600C Treatment in Women With Overactive Bladder

BILADY
Start date: November 2007
Phase: Phase 2
Study type: Interventional

The primary objective of this study is to evaluate the efficacy of SSR240600C in women with overactive bladder compared to placebo using tolterodine as a study calibrator.

NCT ID: NCT00561314 Completed - Prostate Cancer Clinical Trials

High-Intensity Focused Ultrasound Ablation in Treating Patients With Localized Prostate Cancer

Start date: July 2007
Phase: Phase 2
Study type: Interventional

RATIONALE: Highly focused ultrasound energy may be able to kill tumor cells by heating the tumor without affecting the surrounding tissue. PURPOSE: This phase II trial is studying the side effects and how well highly focused ultrasound energy works in treating patients with localized prostate cancer.

NCT ID: NCT00551551 Completed - Clinical trials for Urinary Incontinence

Prenatal Pelvic Floor Prevention (3PN)

Start date: November 2007
Phase: Phase 3
Study type: Interventional

Objective: Compare pelvic floor disorders (urinary incontinence, anal incontinence, genital prolapse, perineal pain, sexual troubles) 12 month after a first delivery between a group of women with prenatal pelvic floor exercises and a control group. Hypothesis: Prenatal pelvic floor exercises reduce postpartum urinary incontinence.

NCT ID: NCT00547378 Completed - Overactive Bladder Clinical Trials

InSite for Over Active Bladder

InSite - OAB
Start date: October 2007
Phase: Phase 4
Study type: Interventional

The purposes of this study are: 1. To provide evidence from a randomized controlled trial that InterStim Therapy provides better relief of symptoms of OAB than standard medical treatments in current use. 2. To fulfill the requirements of the FDA-mandated post-approval study of the safety of the tined lead using a minimally invasive approach.

NCT ID: NCT00535301 Completed - Clinical trials for Urinary Incontinence

Outcomes of Anterior Colporrhaphy Versus Graft Reinforced Anterior Prolapse Repair

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

The purpose of this study is determine whether grafted anterior vaginal prolapse repair is more effective and associated with less complications than prolapse repair with suture.

NCT ID: NCT00534365 Completed - Clinical trials for Stress Urinary Incontinence

Study Comparing TVT With TVT-SECUR for the Treatment of Stress Urinary Incontinence

SECURiTy
Start date: August 2007
Phase: Phase 3
Study type: Interventional

The purpoe of this study is to compare the safety and efficacy of the tension-free vaginal tape procedure (TVT) to the TVT-SECUR procedure in the treatment of stress urinary incontinence.

NCT ID: NCT00506766 Completed - Clinical trials for Urinary Incontinence

Promoting Self Care to Prevent Urinary Incontinence (UI): A Four-Year Follow-up

Start date: September 2000
Phase: Phase 3
Study type: Interventional

This study examined whether self-efficacy promoted adherence to Pelvic Floor Muscle Training (PFMT) and Bladder Training (BT) in women aged 55 and older.

NCT ID: NCT00506116 Completed - Clinical trials for Urinary Incontinence

Promoting Effective Recovery From Labor Urinary Incontinence (PERL)

PERL
Start date: July 1996
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine whether pushing during labor that is controlled by the woman results in less birth-related injury and less postpartum urinary incontinence (UI).

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.