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Urinary Incontinence, Urge clinical trials

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NCT ID: NCT01971437 Completed - Clinical trials for Urinary Incontinence, Urge

Cystoscopy and Cystodistension; Therapeutic and Aetiological Aspect in Overactive Bladder

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

This is an ethically approved randomised controlled study looking at whether Cystodistension(filling the bladder with fluid under pressure) provides any benefit over cystoscopy alone (looking in the bladder) in women with refractory overactive bladder. Urine samples will also be assessed for underlying infected cause of OAB using urinalysis, microscopy and culture and cytokine assays (In collaboration with the University of Kent). We hypothesize that Cystodistension has a therapeutic benefit to women with refractory OAB and the there is an increase prevalence in chronic urinary infections with raised cytokines in women with refractory OAB.

NCT ID: NCT01959347 Completed - Clinical trials for Urinary Incontinence, Stress

Combined Treatment for Mixed Incontinence

ESTEEM
Start date: October 28, 2013
Phase: Phase 3
Study type: Interventional

The overarching goal of this randomized trial is to estimate the effect of combined midurethral sling (MUS) and peri-operative behavioral/pelvic floor therapy (BPTx) compared to MUS alone on successful treatment of MUI symptoms in 472 women. Secondary objectives include estimating the effect of combined treatment compared to MUS on improving overactive bladder (OAB) and stress urinary incontinence (SUI) outcomes separately, need for additional treatment, time to failure and identifying predictors of poor outcomes in this MUI population. A supplemental study, The Human Microbiome Study of ESTEEM, will evaluate the urinary and vaginal microbiome as it relates to women with MUI, their treatment and unaffected controls.

NCT ID: NCT01957137 Completed - Clinical trials for Urinary Urge Incontinence

InterStim® Sacral Nerve Modulation Cycling Study

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

The study will assess the effects of different InterStim cycling settings on urinary urge incontinence.

NCT ID: NCT01829425 Completed - Clinical trials for Urinary Incontinence, Urge

Brain-Centered Therapy Versus Medication for Urgency Urinary Incontinence : Hypnotherapy Or Pharmacotherapy

Hyp-hOP
Start date: April 22, 2013
Phase: N/A
Study type: Interventional

This study is randomized controlled trial in which urgency incontinent women (approximately 150-160) will be randomized to hypnotherapy or pharmacotherapy and evaluated at months 2, 6 &12 Hypotheses: Among patients with urgency urinary incontinence (UUI), hypnotherapy will be non-inferior pharmacotherapy in diminishing UUI episodes. Hypnotherapy may be superior or may not differ from pharmacotherapy in diminishing symptoms or quality of life based on validated questionnaires and/or other diary parameters.

NCT ID: NCT01786967 Completed - Clinical trials for Urge Urinary Incontinence

Understanding the Response to Fesoterodine Through Genetic Evaluation in the Elderly (URGE)

URGE
Start date: September 2012
Phase: Phase 3
Study type: Interventional

Urge urinary incontinence, characterized by unpredictable and embarrassing large volume urine leakage, is a major health issue for elderly women, as it is incredibly common and significantly impairs quality of life. Although anticholinergic medications are the most common therapy, the investigators are unable to predict an individual's response to a particular drug in terms of both effectiveness and side effects. Through genetic evaluation, the investigators have the potential to personalize and optimize drug therapy for millions of elderly women suffering from urge incontinence.

NCT ID: NCT01672190 Completed - Clinical trials for Urinary Incontinence

Lessening Incontinence by Learning Yoga

LILY
Start date: August 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the feasibility of recruiting women with urinary incontinence into a randomized controlled trial of a yoga therapy program.

NCT ID: NCT01644409 Completed - Overactive Bladder Clinical Trials

Urgent-SQ in Treatment of Overactive Bladder Syndrome: 9-yr Follow up

Start date: January 2012
Phase: N/A
Study type: Observational

Long term open label study on safety and durability of the Urgent-SQ tibial implant device for refractory overactive bladder syndrome (OAB).

NCT ID: NCT01619995 Completed - Clinical trials for Urge Urinary Incontinence

Brain Imaging Plus Urodynamics to Investigate the Brain's Control of the Bladder

NIRS/fBFB
Start date: August 2011
Phase: N/A
Study type: Observational

The goal of this project is to evaluate the applicability of non-invasive optical imaging for the measurement of brain function during investigation of the lower urinary tract.

NCT ID: NCT01559389 Completed - Clinical trials for Urge Urinary Incontinence

Incontinence & Intimate Partners: Assessing the Contribution of Treatment

IIMPACT
Start date: March 9, 2012
Phase: Phase 4
Study type: Interventional

Urge urinary incontinence (UUI) is a socially debilitating disease due to its inherently unpredictable nature and sometimes large volumes of urine loss. Women with UUI may experience anxiety over public episodes of incontinence and concerns about odor and, as a result, isolate themselves socially. This isolation affects both partners in the relationship and may be a source of discord. The impact of UUI also moves into personal relationships where fears or actual episodes of incontinence during physical intimacy, including but limited to intercourse, may result in limited interactions and changes in the relationship satisfaction for both partners. Few studies have examined the role of urinary incontinence, particularly UUI, in the dynamics of an intimate partner relationship and none have evaluated the impact of successful UUI treatment. The long-term goal of our research is to understand the social and emotional impact of pelvic floor disorders, particularly UUI, on the well-being of an intimate relationship. Ultimately, we aim to evaluate the role that successful treatment plays in the alleviation of discord in intimate partner relationships that are affected by UUI and other pelvic floor disorders. Our objective for this proposal is to characterize, using validated, quantifiable methods the quality of the relationship in couples affected by UUI and to identify the role that treatment plays in improving this relationship. Our central hypothesis is that UUI has a negative impact upon the emotional and physical well-being of a relationship and that effective treatment will result in improvement in areas of the relationship that have been detrimentally affected by UUI. Our rationale for this study is that an understanding of UUI in the context of a couple, particularly from the perspective of the male partner, will improve our ability to holistically treat UUI, thus improving patient outcomes and satisfaction.

NCT ID: NCT01512004 Completed - Overactive Bladder Clinical Trials

Propiverine Hydrochloride Extended-Release Capsule for Overactive Bladder

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

The purpose of this Phase III study is to evaluate the efficacy and safety of Propiverine Hydrochloride Extended-Release Capsule in the treatment of overactive bladder in Chinese population with urgent micturition, frequent micturition and/or urge urinary incontinence.