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Enuresis clinical trials

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NCT ID: NCT02511314 Completed - Clinical trials for Urinary Incontinence

A Trial of effectIveness of a Smart Sensor for Continence Care: the ARCTICC Study

ARCTICC
Start date: January 2, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the use of an electronic incontinence identification system with nursing home support (Tena Identifi) versus usual care on the quality, resource use and outcomes of continence care for older residents of nursing care homes.

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: NCT02506309 Completed - Clinical trials for Urinary Incontinence, Stress

Trans-obturator Mid-urethral Sling and the Single-incision Sling in Women With Stress Urinary Incontinence

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

Mid-urethral slings (MUS) now represent a gold standard in the treatment of female stress urinary incontinence (SUI). Second generation trans-obturator slings (TOT) have proven to be as effective as retropubic tension-free vaginal tape (TVT) with fewer major complications. A third generation of the MUS inserted through a single vaginal incision (SIS) has become a means to overcome significant post-operative groin pain. Novel types of SIS with a more robust and adjustable anchoring mechanism can assure adequate long-lasting attachment to the obturator membrane (OM). Objective of this study was to compare an inside-out TOT with an innovative fixation SIS in randomized controlled trial on patients undergoing their primary surgery for urodynamic SUI.

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: 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: NCT02476175 Completed - Clinical trials for Urinary Incontinence

Add-on Mirabegron in Pediatric Patients With Refractory Overactive Bladder

Add-on-Mira
Start date: April 2013
Phase: Phase 3
Study type: Interventional

The objective is to evaluate the efficacy and safety of adding mirabegron to an antimuscarinic to treat urinary incontinence in children with Overactive Bladder that are refractory to antimuscarinics.

NCT ID: NCT02468830 Completed - Clinical trials for Urinary Incontinence

Pilot Study of Mirabegron in Pediatric Patients With Overactive Bladder

Mirabegron
Start date: April 2013
Phase: Phase 3
Study type: Interventional

The objective is to evaluate the efficacy and safety of mirabegron to treat urinary incontinence in children with Overactive Bladder that are refractory and/or intolerant to antimuscarinics.

NCT ID: NCT02453100 Completed - Clinical trials for Urinary Incontinence

Managing Urinary Incontinence in Elderly Village Women in Rural Bangladesh

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

An intervention consisting of group and home based exercise will be used over 6 months to assess whether this is helpful in managing urinary incontinence in elderly village women in Bangladesh. This intervention, supplemented by education about managing incontinence, will be used in half the villages in the trial. In the other half women will receive only the education component.

NCT ID: NCT02446808 Active, not recruiting - Clinical trials for Urinary Incontinence

Intraoperative Nerve Monitoring During Robot-assisted Laparoscopic Prostatectomy

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

The purpose of this study is to determine whether the use of intraoperative nerve monitoring during robotic-assisted laparoscopic prostatectomy surgery improves post-surgery urinary continence and erectile function.

NCT ID: NCT02443987 Unknown status - Clinical trials for Stress Urinary Incontinence

Time Interval Between TVT and First Void (TIBT) Study

TIBT
Start date: May 2015
Phase: N/A
Study type: Interventional

The primary aim of this study is to compare, in women undergoing tension-free vaginal tape (TVT) insertion under sedation and local anaesthetic infiltration, the time interval of first void following surgery between a group of patients who received intravenous fluids to those who did not.