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Urinary Incontinence, Stress clinical trials

View clinical trials related to Urinary Incontinence, Stress.

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NCT ID: NCT02334878 Completed - Clinical trials for Urinary Incontinence, Stress

Stem Cell Therapy for Treatment of Female Stress Urinary Incontinence

Start date: October 1, 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the effectiveness of mesenchymal stem cells in treatment of stress urinary incontinence due to intrinsic sphincter deficiency; in which the problem is weakness or damage of the sphincter muscle responsible for continence. Mesenchymal stem cells are undifferentiated cells which can undergo self-renewal & differentiation into other cell types like muscle cells; thus can be used to regenerate the damaged sphincter muscles. In this study mesenchymal stem cells will be obtained from bone marrow from the patient, processed, & then re-injected periurethrally. Effectiveness will be compared to that of the surgical treatment (tension-free vaginal tape).

NCT ID: NCT02319096 Completed - Clinical trials for Urinary Stress Incontinence

Vibration Training and Pelvic Floor Muscle Strength in Females With Stress Urinary Incontinence

Start date: December 2014
Phase: N/A
Study type: Interventional

Pelvic floor muscle training (PFMT) is the first line therapy recommended by NICE for the treatment of SUI. Due to poor motivation and compliance only 15-20% of women comply with the regimen. Whole body vibration (WBV) exercise has been developed as a new modality in the field of physiotherapy. The Galileo machine is a unique device for applying whole-body vibration. The investigators are currently using this therapy as an alternative to traditional pelvic floor muscle therapy. The investigators aim to audit the investigators treatment of whole body vibration.

NCT ID: NCT02318251 Active, not recruiting - Clinical trials for Urinary Incontinence, Stress

Stress Urinary Incontinence Physiotherapy

Start date: January 2015
Phase: N/A
Study type: Interventional

The purpose of the present study is to compare two different physiotherapy programs regarding their effect on stress urinary incontinence.

NCT ID: NCT02316275 Recruiting - Clinical trials for Stress Urinary Incontinence

Impact of Unrestrictive Exercise Following Mid-Urethral Sling Surgery

Start date: December 2011
Phase: N/A
Study type: Interventional

To determine the impact of unrestricted postoperative activity on intermediate- and long-term continence outcomes of mid-urethral sling surgery in women with stress urinary incontinence. To assess the natural return to baseline activity level when patients are unrestricted following mid-urethral sling surgery with or without concomitant anterior or posterior pelvic organ prolapse repair.

NCT ID: NCT02296099 Completed - Clinical trials for Urinary Incontinence, Stress

Trial Liposomal Bupivacaine Following Retropubic Suburethral Sling for Stress Urinary Incontinence

Start date: November 2014
Phase: Phase 4
Study type: Interventional

The purpose of the study is to determine if the administration of liposomal bupivacaine at the completion of a suburethral sling procedure will result in decreased postoperative pain compared to no injection.

NCT ID: NCT02291432 Completed - Stress Clinical Trials

Autologous Cell Therapy for Stress Urinary Incontinence in Males Following Prostate Surgery

Start date: February 19, 2015
Phase: Phase 1/Phase 2
Study type: Interventional

To study the safety and potential efficacy of Autologous Muscle Derived Cells for Urinary Sphincter Repair (AMDC-USR) for the treatment of male stress urinary incontinence (SUI) for patients that have undergone prior prostate surgery.

NCT ID: NCT02288455 Completed - Clinical trials for Male Stress Urinary Incontinence

Clinical Investigation of GT UrologIcal, LLC's Artificial Urinary Sphincter (RELIEF II)

RELIEFII
Start date: October 2014
Phase: N/A
Study type: Interventional

The purpose of this investigation is to demonstrate the safety and efficacy of the GTU artificial urinary sphincter device in restoring continence in males who have confirmed urinary stress incontinence for a minimum of 12 months with primary etiology being radical prostatectomy or transurethral resection of the prostate (TURP).

NCT ID: NCT02277288 Recruiting - Clinical trials for Stress Urinary Incontinence

Does Bladder Instillation Reduce Time to Discharge After Sling Surgery

Start date: December 2011
Phase: N/A
Study type: Interventional

The purpose of this randomized control trial study is to determine if intraoperative bladder instillation of fluid decreases the time to discharge after having an outpatient mid-urethral sling procedure, and to measure the cost savings of this decrease in hospital stay. Charges will be broken down between recovery room charges and discharge area, as recovery room charges are significantly higher. The investigators suspect that a shorter time in the recovery room will translate into fewer charges.

NCT ID: NCT02275728 Active, not recruiting - Menopause Clinical Trials

Pelvic Floor Muscle Training With and Without Biofeedback in Women With Stress Urinary Incontinence

Start date: May 2014
Phase: N/A
Study type: Interventional

This study evaluates the action of the pelvic floor muscle training with and without EMG Biofeddback in the treatment of stress urinary incontinence in menopausal, peri and post menopausal women and their quality of life before and after the interventions.

NCT ID: NCT02263534 Completed - Clinical trials for Stress Urinary Incontinence

Comparing Minisling to Tension Free Vaginal Tape in Mangement of Stress Urinary Incontinence

Start date: November 10, 2014
Phase: Phase 2/Phase 3
Study type: Interventional

Based on previous studies the single incision minisling is an easy less invasive procedure with fewer complications and cure rate similar to conventional midurethral slings in the treatment of female stress urinary incontinence. The aim of this study is to test the hypothesis that the single incision mini-sling placed in the "U" position is not inferior to TVT in this patient population.