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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT03296748 Completed - Clinical trials for Stress Urinary Incontinence

Correction of Asymptomatic 2nd Degree Cystocele in Patient With Stress Incontinence

Start date: June 1, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

The aim of our study is to assess the value of concomitant surgical correction of asymptomatic grade II anterior vaginal wall prolapse with the placement of midurethral sling for treatment of female patients with stress incontinence

NCT ID: NCT03296462 Completed - Clinical trials for Urinary Incontinence, Stress

Hip External Rotation Physical Therapy Trial

HER-Physio
Start date: November 3, 2016
Phase: N/A
Study type: Interventional

This RCT is a feasibility study to evaluate the Lois Hole Hospital for Women's Urogynecology Clinic's ability to recruit and randomize SUI patients to the proposed RCT, and to test the study procedures and follow-up schedule for participants. The study interventions used in the feasibility study will be training of (1) Hip Extension Rotation (HER) exercises alone, (2) HER exercises in combination with Pelvic Floor Muscle (PFM) exercises, or (3) PFM exercises alone (control/usual care) in the treatment of SUI.

NCT ID: NCT03296241 Completed - Clinical trials for Stress Urinary Incontinence

Non-ablative Er:Yttrium Aluminum Garnet Laser for Stress Urinary Incontinence (SUI)

Start date: August 1, 2012
Phase: N/A
Study type: Interventional

Stress urinary incontinence (SUI) is a common complaint in women after childbirth. The aim of this study was to evaluate the efficacy and safety of non-ablative Er:YAG laser therapy in the treatment of SUI and improvement of sexual gratification in parous women. 114 premenopausal parous women with SUI were randomized in two groups of 57 women; a laser intervention group and sham control (placebo) group. Both groups were treated according to the IncontiLaseTM clinical treatment protocol for SUI with non-ablative thermal-only Er:YAG laser, except that there was no energy output when treating the sham group. Patients were blinded to the allocation. At baseline and 3 months after treatment patients were clinically examined, answered questionnaires for SUI severity sexual function assessment and their pelvic floor muscle (PFM) function was assessed with perineometry. The improvement in the laser group will be compared to the improvement in the sham group.

NCT ID: NCT03295487 Completed - Clinical trials for Stress Urinary Incontinence

ToT and Estrogen in Postmenopausal Females

Start date: March 1, 2017
Phase: Phase 2/Phase 3
Study type: Interventional

To compare the subjective and objective outcomes of TVT-O procedure alone versus the same procedure followed by the use of premarin vaginal cream for 3 months in postmenopausal female with genuine stress incontinence.

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.