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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT01095692 Completed - Clinical trials for Pelvic Organ Prolapse

Evaluating the Necessity of TOT Implantation in Women With Pelvic Organ Prolapse and Occult Stress Urinary Incontinence

ATHENA
Start date: July 2010
Phase: N/A
Study type: Interventional

Nowadays the clinical significance of an occult stress urinary incontinence and its optimal treatment is not known.Regarding treatment, there are 2 main approaches : either the systematic preventive treatment of the occult stress urinary incontinence by means of a tension free vaginal tape (TOT) together with the treatment of prolapse or the treatment of prolapse in the first place and treatment of stress incontinence in a second time when and if it appears.This study is expected to provide objective evidence concerning the efficacy and security of TOT implantation for the prevention treatment of occult stress urinary incontinence in women with pelvic organ prolapse and occult urinary incontinence.The perspective is to improve the management of these patients by providing evidence based recommendation for their treatment.

NCT ID: NCT01095159 Completed - Clinical trials for Stress Urinary Incontinence

TVTO™ X TVTS ™ for Treatment of Stress Urinary Incontinence

TVTOxTVTS
Start date: February 2009
Phase: Phase 4
Study type: Interventional

This is a prospective, comparative randomized controled trial. The general purposes of this study is to compare the efficacy and safety of TVTO™ and TVTSecur™ as surgical treatment for female urinary stress incontinence.

NCT ID: NCT01094353 Completed - Clinical trials for Female Stress Urinary Incontinence

A Comparative Study Minisling Versus Transobturator (TOT)Sling

sui
Start date: June 2008
Phase: Phase 4
Study type: Interventional

A study to compare efficacy in surgical treatment for SUI (Stress Urinary Incontinence), tot with minisling.

NCT ID: NCT01073878 Completed - Clinical trials for Urinary Incontinence

Athena Pelvic Muscle Trainer - DUETS Trial

DUETS
Start date: February 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine if the Athena Pelvic Muscle Trainer device effectively treats stress, urge or mixed incontinence in women by strengthening the pelvic floor muscles by collecting data from the patient on the 1. Over Active Bladder Questionnaire 2. The 7-Day Urine Diary questionnaire This study will also look at whether or not there is an improvement in sexual health after using the device by collecting data frm the patient on the 3. Female Sexual Function Index questionnaire

NCT ID: NCT01069484 Completed - Clinical trials for Urinary Incontinence

Postpartum Pelvic Floor Muscle Training in Women With and Without Injured Pelvic Floor Muscles

PP-PFMT
Start date: February 2010
Phase: Phase 3
Study type: Interventional

Although pregnancy and childbirth are associated with happiness and a positive life change for most women, it can also be considered as risk periods for injuries to the pelvic floor and development of pelvic floor dysfunction. This may leed to devastating loss of function and quality of life (Ashton-Miller & DeLancey 2007). The aim of this study is to evaluate the effect of postpartum pelvic floor muscle training for primiparous women with and without pelvic floor muscle injury.

NCT ID: NCT01067261 Completed - Clinical trials for Urinary Incontinence

Transcutaneous Mechanical Nerve Stimulation (TMNS) by Vibration in the Preservation and Restoration of Urinary Continence and Erectile Function and in the Treatment of Erectile Dysfunction and Urinary Incontinence in Conjunction With Nerve Sparing Radical Prostatectomy

Start date: February 2010
Phase: Phase 3
Study type: Interventional

After radical prostatectomy nerve damage in the pelvic floor usually occurs. This causes side effects in the form of incontinence and erectile dysfunction. It has previously been shown that one can stimulate the nerves of the pelvic floor by means of transcutaneous mechanical nerve stimulation (TMNS) done through vibration. This study will examine the effect of TMNS in the preservation and restoration of urinary continence and erectile function and in the treatment of urinary incontinence and erectile dysfunction in conjunction with radical prostatectomy. The theory is that by means of TMNS one can stimulate the nerves of the pelvic floor and the penis which may improve their function and there by prevent or minimize the occurrence of incontinence and erectile dysfunction following pelvic surgery. Vibration may also help to eliminate these symptoms once they have occurred. It is possible that TMNS will also directly increase the blood flow in the cavernosal tissue thus aiding in the preservation of this tissue. In case the improved nerve function is not great enough to secure satisfactory erectile function in itself it may still improve the effect of PDE-5-inhibitors. In pilot studies TMNS has already shown an effect in the treatment of urinary continence. In this study the patients will be randomized to either TMNS treatment or no TMNS treatment. In both groups the patients will participate in a pelvic floor muscle training program. In the group receiving active treatment this will be supplemented by TMNS treatment. The two groups will be evaluated and compared with regard to erectile function time to continence after surgery.

NCT ID: NCT01066117 Not yet recruiting - Clinical trials for Urinary Incontinence

Effectiveness of PeeRelease - a Gel Absorbent Pad in Moderate to Severe Urinary Incontinence

Start date: February 2010
Phase: N/A
Study type: Interventional

The purpose of the proposed study is to test the effect of the new gel pad on the quality of life of urinary incontinent men and women and to assess to what extent the gel pad improves the quality of life of incontinence persons.

NCT ID: NCT01057550 Completed - Clinical trials for Stress Urinary Incontinence

Randomised Controlled Trial Comparing Tension-Free Vaginal Tape (TVT), Pelvicol & Autologous Slings for Stress Urinary Incontinence(SUI)

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

The purpose of this trial was to discover which type of operation for stress urinary incontinence in women offered better results: autologous slings, TVT or Pelvicol slings.

NCT ID: NCT01056666 Completed - Clinical trials for Urinary Incontinence

Conveen Optima Urisheaths With Collecting Bags Versus Absorbents

Start date: June 2007
Phase: Phase 4
Study type: Interventional

The objective of this investigation is to asses with validated scales, the impact on the quality of life of men suffering of moderate to severe incontinence of the use of Conveen Optima urisheath in comparison with their usual absorbent protection.

NCT ID: NCT01055860 Completed - Clinical trials for Urinary Incontinence

One Year Outcome After Robotic Assisted Laparoscopic Sacral Colpopexy, a Case Series Review

Start date: February 2009
Phase: N/A
Study type: Observational

Robotic approach to sacral colpopexy is a relatively new procedure. The literature is scarce in regard to its long-term outcomes. This advanced procedure is offered at MMH through the Urogynecology division. The Investigators setup to review the one year outcome of patients who underwent this procedure using a polypropylene mesh. These outcomes will include anatomical and quality of life measures.