Clinical Trials Logo

Stress Urinary Incontinence clinical trials

View clinical trials related to Stress Urinary Incontinence.

Filter by:

NCT ID: NCT02049840 Completed - Clinical trials for Stress Urinary Incontinence

The European Study of Altis Single Incision Sling System for Female Stress Urinary Incontinence

EASY
Start date: December 16, 2013
Phase: N/A
Study type: Interventional

This is a prospective, post-market, single arm, multicenter study comparing Baseline data to the 12 month and 36 month data in 136 female patients with Stress Urinary Incontinence

NCT ID: NCT01948713 Completed - Clinical trials for Stress Urinary Incontinence

Effect of Pelvic Floor and Hip Muscle Strengthening in the Treatment of Stress Urinary Incontinence

Start date: January 7, 2013
Phase: N/A
Study type: Interventional

INTRODUCTION: Stress urinary incontinence is a common condition in women and can be defined as the involuntary loss of urine on exertion, exercise, sneezing or coughing. This pathology causes physical discomfort and impacts the quality of life in a negative manner. Physiotherapeutic exercises is a treatment with low cost and high patient attendance. It can be applied with focus on strengthening the pelvic floor muscles or on muscular synergism. OBJECTIVE: To compare the effectiveness of Kegel exercises performed alone or performed in association with the strengthening of the muscles of the hip in the treatment of stress urinary incontinence. METHODOLOGY: The study is a randomized, blinded clinical trial. It aims at assessing objectively the strength of the pelvic floor, the improvement in the number of episodes of loss and impact on quality of life. The study will accept up to 40 women, who will be divided into two groups of physical therapy: group 1 (that will strengthen the pelvic floor muscles with Kegel exercises) and group 2 (that will perform strengthening the pelvic floor muscles with Kegel exercises associated with the strengthening of muscles of the hip). The two groups will be evaluated at the beginning and at the end of treatment.

NCT ID: NCT01924728 Completed - Clinical trials for Stress Urinary Incontinence

Efficacy of Magnetic Stimulation for Stress Urinary Incontinence

Start date: September 2013
Phase: N/A
Study type: Interventional

The aim of the study is to investigate the effects of QRS®-1010 PelviCenter in female patients with stress urinary incontinence. Based on the available data on magnetic stimulation, the investigators hypothesize that magnetic stimulation via QRS®-1010 PelviCenter will reduce the number and amount of urinary leakage upon exertion as well as improve patients' quality of life.

NCT ID: NCT01893138 Completed - Clinical trials for Stress Urinary Incontinence

Autologous Muscle Derived Cells for Female Urinary Sphincter Repair

Start date: November 21, 2013
Phase: Phase 3
Study type: Interventional

This randomized, double-blind, placebo-controlled, multicenter, confirmatory study will evaluate the efficacy and safety of Cook MyoSite Incorporated Autologous Muscle-Derived Cells (generic name Iltamiocel) compared to a placebo (vehicle) control dose in the treatment of stress urinary incontinence (SUI) in adult female patients.

NCT ID: NCT01866085 Recruiting - Clinical trials for Stress Urinary Incontinence

AdVance® vs ARGUS® Sling Procedure in Male With Post Prostatectomy Stress Urinary Incontinence

Start date: June 2012
Phase: N/A
Study type: Interventional

The study is designed to assess efficacy and subject satisfaction of two sling devices: Advance and Argus, in male patients with stress urinary incontinence after prostatectomy.

NCT ID: NCT01850342 Enrolling by invitation - Clinical trials for Stress Urinary Incontinence

Effectiveness and Safety of Cell-Assisted Lipotransfer for the Treatment of Stress Urinary Incontinence

Start date: May 2013
Phase: Phase 1/Phase 2
Study type: Interventional

Autologous washed and homogenized fat micrograft harvested from the patient's front abdominal wall enriched with adipose-derived regenerative cells (ADRC) derived by enzyme-treatment of a portion of the harvested fat. Fat tissue micrograft mixed with ADRC will be administered one-time endoscopically into submucosal layer of urethra under eye control. This is a single arm study with no control. All patients receive cell therapy.

NCT ID: NCT01799122 Not yet recruiting - Clinical trials for Stress Urinary Incontinence

Trial Comparing Mini-Arc Precise Pro and the Trans Vaginal Obturator Tape for Stress Urinary Incontinence

Start date: n/a
Phase: Phase 3
Study type: Interventional

Randomized comparison of two surgeries for the treatment of female stress urinary incontinence.

NCT ID: NCT01784588 Completed - Clinical trials for Stress Urinary Incontinence

Post Market Study Of Single Incision Sling Versus Transobturator Sling for Stress Urinary Incontinence

Solyx
Start date: June 2013
Phase: N/A
Study type: Interventional

The purpose of this research study is to compare the treatment device (Solyx) to a different mesh sling or control device (Obtryx II) for the treatment of symptoms for Stress Urinary Incontinence (SUI). Safety information and patient outcomes will be collected for three (3) years and evaluated.

NCT ID: NCT01770691 Completed - Clinical trials for Stress Urinary Incontinence

Preliminary Performance Study of the New TIPI Device in the Prevention of Stress Urinary Incontinence

Start date: September 2007
Phase: N/A
Study type: Interventional

Stress urinary incontinence (SUI) is most prevalent among women. SUI is characterized by loss of urine from increased abdominal pressures caused by coughing, laughing, sneezing, running, lifting or walking. SUI cause women to avoid routine physical activities, thus detracting significantly from their quality of life. The purpose of this study is to evaluate the performance of new designs of the TIPI device, a conservative, disposable, treatment for temporary management of SUI.

NCT ID: NCT01763957 Withdrawn - Quality of Life Clinical Trials

Paula Method Compared to Pelvic Floor Muscle Training (PFMT), for Urinary Stress Incontinence

Start date: March 2013
Phase: N/A
Study type: Interventional

The Investigators decided to examine whether the Paula method is more effective than Pelvic Floor Muscle Training (PFMT) in terms of urinary leakage amount, as it measured by pad test in menopause women without an hormonal therapy. In addition to the pad test and two urinary incontinence questionnaires, we will use other assessment tools such as; quality of life and sexual function which have been found to correlate significantly with pad test results. These results may indicate that menopausal women with Stress Urinary Incontinence may be more successful controlling incontinence if they will practice the Paula method as compared to PFMT.