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Enuresis clinical trials

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NCT ID: NCT03289117 Completed - Anesthesia, Local Clinical Trials

Evaluation of a Novel Medical Device to Facilitate Gel Instillation During Change of Long-term Urinary Catheters

Start date: April 17, 2016
Phase: N/A
Study type: Interventional

A randomized, open label, controlled, parallel group study to investigate difference between regional standard procedure and a novel modified procedure (using an additional novel device to facilitate gel installation) for changing long-term indwelling urinary catheters.

NCT ID: NCT03273309 Completed - Clinical trials for Urinary Incontinence

Comparison of Vibratory Perineal Stimulus With Transvaginal Electrical Stimulation

Start date: June 1, 2017
Phase: N/A
Study type: Interventional

Aim: To compare the effects of Vibratory Perineal Stimulus with transvaginal electrical stimulation to the pelvic floor muscles functionality in women with urinary incontinence and who are unable to voluntarily contract their pelvic floor muscles. Study Design: Randomized controlled trial

NCT ID: NCT03265509 Completed - Clinical trials for Urinary Incontinence

Effect of Glutamine on Urinary Incontinence

Start date: January 2016
Phase: N/A
Study type: Interventional

The objective of this study is to determine to effect of additional oral glutamine to Kegel exercises on pelvic floor strength and clinical parameters of urinary incontinence in females with either urinary incontinence (stress and/or urgency) and pelvic prolapse.

NCT ID: NCT03263676 Completed - Clinical trials for Reusable Underwear, Urinary Incontinence, Dispoable Pad

Randomized Controlled Crossover Comparison of Icon Underwear to Disposable Pads

Start date: July 1, 2016
Phase: N/A
Study type: Interventional

This is a randomized cross over trial to compare quality of life and product performance between Icon reusable underwear versus standard disposable pad in patients with mild to moderate urinary incontinence.

NCT ID: NCT03256565 Completed - Clinical trials for Stress Urinary Incontinence

Q-tip Test and Urodynamic Study

Start date: June 30, 2017
Phase:
Study type: Observational

Urethral hypermobility, which can be assessed with Q-tip test, has been considered to be partly responsible for pathogenesis of women with stress urinary incontinence (SUI). Nonetheless, Q-tip test has lost favor due to patient discomfort. Thus, the purpose of this study was to search a surrogate for assessment of urethral hypermobility by correlating the Q-tip angle and the urodynamic variables in women with SUI.

NCT ID: NCT03254355 Completed - Clinical trials for Urinary Incontinence

Efficacy of Physiotherapy for Urinary Incontinence in Women With a Puborectalis Avulsion

Start date: August 28, 2017
Phase: N/A
Study type: Interventional

Childbirth is a major risk factor for pelvic floor muscle (PFM) trauma. In one third of women, stretching of the PFM will result in an avulsion injury (i.e. disconnection of the muscle from its insertion points on the pubic symphysis). Recent advances in imaging have led to the discovery of this previously unknown major injury and further research now enables its diagnosis with readily available techniques. Avulsion injury has alarming consequences because it has been associated with a higher rate of urinary incontinence in the postpartum period as well as the long-term development of other major urogynecological conditions such as pelvic organ prolapse and anal incontinence. Women with avulsion not only suffer from severe symptoms with significant related impacts on physical activities, overall well-being and quality of life, but they also present a higher rate of surgical failures. Moreover, it is still unknown whether the most recommended first-line treatment for urinary incontinence -PFM physiotherapy- is effective in women with this major trauma. Until now, only a pilot study conducted by our team supports the rationale and the efficacy of physiotherapy for improving PFM function in women with avulsion, despite their major muscle injury. Primary objective: To evaluate the efficacy of physiotherapy for urinary incontinence in women with avulsion at 9-months after randomization compared to a waiting-list control group. Secondary objectives: 1. To compare physiotherapy to the control group after treatment and at 9-months after randomization in terms of: a) incontinence and prolapse (objective quantification, symptoms and related impact); b) PFM morphology and function; c) sexual function; d) self-efficacy; e) cost analysis; f) treatment satisfaction and impression of change. 2. To investigate the impact of the severity of the avulsion (i.e. unilateral or bilateral) on the response to physiotherapy treatment on the aforementioned outcomes.

NCT ID: NCT03250988 Completed - Clinical trials for Nervous System Diseases

Prevalence of Comorbid Spasticity and Urinary Incontinence in Residents of a Long-Term Care Facility

Start date: January 30, 2018
Phase:
Study type: Observational

The purpose of this study is to improve spasticity diagnosis through exploration of potential new diagnostic markers for spasticity that can assist in diagnosis and referral.

NCT ID: NCT03241342 Completed - Clinical trials for Stress Urinary Incontinence

Study to Assess Enobosarm (GTx-024) in Postmenopausal Women With Stress Urinary Incontinence

ASTRID
Start date: August 21, 2017
Phase: Phase 2
Study type: Interventional

GTx-024 is an orally bioavailable and tissue-selective nonsteroidal selective androgen receptor modulator (SARM) that has demonstrated androgenic and anabolic activity and is currently being evaluated as a potential treatment for stress urinary incontinence (SUI) in postmenopausal women. Urinary incontinence and pelvic floor disorders are major health problems for women, especially as they age. Pelvic floor muscle relaxation has been found to correlate with lower urinary tract symptoms including SUI. Muscles of the pelvic floor and lower urinary tract are crucial for supporting the pelvic organs and micturition; however, damage to the muscles or lack of hormonal stimulation are thought to contribute to pelvic organ prolapse and urinary incontinence. Although anabolic steroids may increase muscle mass and strength, lack of oral bioavailability and known potential risks have limited their use. Nonsteroidal SARMs have potential to achieve benefits of anabolic steroid therapy (improved muscle mass, cholesterol/triglyceride levels, glucose metabolism, and bone density) with fewer adverse effects, such as hirsutism and acne, in women. Both nonclinical and clinical data suggest that SARMs may provide a new therapeutic option for pelvic floor and lower urinary tract disorders, as both testosterone and its more potent metabolite, dihydrotestosterone, have anabolic effects on muscle.

NCT ID: NCT03221725 Completed - Clinical trials for Pelvic Organ Prolapse

The Development of De-novo Stress Urinary Incontinence After Stage II-III Pelvic Organ Prolapse Surgery

Start date: February 1, 2017
Phase: N/A
Study type: Interventional

Surgery for Stage II-III Pelvic organ prolapse

NCT ID: NCT03209570 Completed - Clinical trials for Urinary Incontinence

A Pilot Clinical Trial of TENA Identifi in the Nursing Home Setting

Start date: October 19, 2017
Phase: N/A
Study type: Interventional

The purpose of this study is to prospectively compare a standard of care manual toileting protocol (e.g., "check and change" strategy) to toileting patterns recorded by the TENA Identifi system in identifying incontinence patterns and events, and, whether such data differentially improve a care planning strategy, nursing effort, product use, and wet-time for urinary incontinence.