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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT02510131 Recruiting - Clinical trials for Urinary Incontinence

Is Hyacinth Exercise Better Than Kegel's Exercise in Women With Urinary Incontinence?

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

To determine whether Hyacinth exercises are more effective than Kegel's exercise at improving pelvic floor weakness among women aged 55 and above with urinary incontinence.

NCT ID: NCT02490917 Recruiting - Clinical trials for Urinary Incontinence

ACT™ Balloons Versus Artificial Urinary Sphincter (AMS800™) for the Treatment of Female Stress Urinary Incontinence

SU-ACT
Start date: September 2015
Phase: N/A
Study type: Interventional

The main objective is to compare the efficacy of AMS800 ™ and ACT ™ devices for the Treatment of Female Stress Urinary Incontinence due to Intrinsic Sphincter Deficiency on "social continence" at 6 months. Continence is defined by the average number of pads used per day. The social continence is defined by (0-1) pad per day

NCT ID: NCT02485665 Recruiting - Exercise Clinical Trials

Efficacy of Extracorporeal Biofeedback Device for Post-prostatectomy Incontinence

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

To evaluate the efficacy of postoperative pelvic floor muscle training using personalized extracorporeal biofeedback device among patients with post-prostatectomy incontinence

NCT ID: NCT02482896 Recruiting - Atherosclerosis Clinical Trials

The Lolland-Falster Health Study

LOFUS
Start date: February 2016
Phase: N/A
Study type: Observational

The study is a epidemiological, cross-sectional study in a mainly rural area of Denmark in Denmark. Life expectancy is shorter, morbidity is higher, and social problems more prevalent than in the urban areas of the country. The population study aims at examining complexities of environmental, hereditary, lifestyle, and social factors as determinants and predisposing factors for morbidity, health, and quality of life. The study will cover physical, mental, and social dimensions and examine family patterns and subgroups. The study will provide baseline information for later follow-up.

NCT ID: NCT02367404 Recruiting - Prostate Cancer Clinical Trials

Prospective RCT on Post Prostatectomy Urine Leak

Start date: May 2015
Phase: Phase 3
Study type: Interventional

Objectives: Primary: Comparison of proportion of patient achieving continence between the four arms at 6 months. Secondary: - Comparison of time to achieve continence between the four arms. - Comparison of urinary symptoms and quality of life improvement between the four arms. - Assessment of adverse events in Duloxetine arms. Primary outcome/ time frame: Proportion of patient achieving continence at 6 months. Continence is defined as "using no pad"or "only security pad". Secondary outcome: - time to achieve continence - Quality of life tested in relation to incontinence according to Visual Analog Scale (VAS) and King's Health Questionnaire (KQH). - Urinary symptoms measured with International Prostate Symptom Score (IPSS). No. of subjects entered: 300 patients informed and included, 240 patients will be randomized. Statistical methods - Proportion of patients who achieve continence and time to achieve continence will be compared between the four arms. - Comparison of quality of life outcomes between the four arms - Comparison of clinical variables that can affect the primary/secondary outcome - univariate and multivariate analysis (ITT).

NCT ID: NCT02331186 Recruiting - Obesity Clinical Trials

Effects of Bariatric Surgery on Pelvic Floor Fonctions in Obese Women

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

Urinary incontinence is well documented as a comorbidity of obesity. Studies demonstrate improvement of incontinency after weight loss. However, the mechanisms are still not clear. Aim of our study to analyze the effects of bariatric surgery on pelvic floor function in women.

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: NCT02301013 Recruiting - Clinical trials for Urinary Incontinence

Impact of Urethral Mobility on the Success of Sling Operations

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

Main objective is to evaluate the relation between the increased urethral mobility and unsuccessful treatment after TVT and TOT operations. 140 patients will be included in the research who are planned to have TVT and TOT operations with SUI and MUI diagnoses.Female patients of 25 to 70 years of age who are positive for stress test will be included. All patients will be questioned for parity, body mass index, menopausal state, medical history, and examined for POP-Q stage, urodynamy, stress test, UDI 6, IIQ7 and with transperineal sonography preoperatively. "Passive mobility angle" and "active mobility angle" will be measured. The relationship between passive mobility angle or active mobility angle and success of sling operations will be determined in this study.

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: NCT02243085 Recruiting - Clinical trials for Urinary Incontinence

Predictors of de Novo Urge Urinary Incontinence After Photoselective Vaporization of the Prostate

Start date: August 2014
Phase: N/A
Study type: Observational

The aim of this study was to investigate the incidence of de novo urge urinary incontinence after the photoselective vaporization of the prostate for benign prostatic hyperplasia using the validated overactive bladder symptom score, and to determine the predictors of de novo urge urinary incontinence following the photoselective vaporization of the prostate.