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Enuresis clinical trials

View clinical trials related to Enuresis.

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NCT ID: NCT02400034 Completed - Clinical trials for Stress Urinary Incontinence

Comparing Voiding Trials After Midurethral Sling for Stress Incontinence

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

Urinary incontinence is a prevalent health and quality of life concern affecting almost half of women over the age of 20. Urinary retention (abnormal holding of urine) is a concern of many surgeons who perform midurethral sling surgery. All patients after outpatient midurethral sling or vaginal prolpase surgery must complete a voiding trial if they are to be discharged without a catheter. The purpose of this study is to compare two different types of postoperative voiding trials to determine which leads to less post-operative issues, such as urinary retention requiring catheterization. You are being asked to participate because you are having midurethral sling surgery, either with or without vaginal prolapse repair.

NCT ID: NCT02369445 Completed - Autistic Disorder Clinical Trials

Investigation of Teacher-Mediated Toilet Training Using a Manualized Moisture Alarm Intervention

Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this pilot study is to compare an innovative toilet training strategy with a standard behavioral intervention in children with autism spectrum disorder (ASD), as implemented by teachers in the school setting. Thirty classrooms with a total of 60 children with ASD (aged 3 - 10 years) will be enrolled in the study. Each classroom will be randomly assigned to either the innovative strategy group or the standard behavioral group. The innovative strategy employs an electronic moisture pager that sends a signal when the child begins having a urine accident. Outcome measures include rate of urine accidents and rate of toilet use in the two groups.

NCT ID: NCT02368262 Completed - Clinical trials for Urinary Incontinence

Prevalence of Incontinence and Risk Factors in Children With Cerebral Palsy

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

This study evaluates (risk)factors influencing (in)continence in children with and without a brain injury.

NCT ID: NCT02364063 Completed - Clinical trials for Daytime Urinary Incontinence

Micturition Reeducation in Children With Cerebral Palsy

Start date: September 2014
Phase: N/A
Study type: Interventional

This study evaluates the effectiveness of a voiding reeducation program as treatment for incontinence in children with a brain injury.

NCT ID: NCT02348112 Completed - Clinical trials for Stress Urinary Incontinence

Altis® 522 Trial - Treatment of Female Stress Urinary Incontinence

Start date: January 2015
Phase:
Study type: Observational

The aim of this postmarket study is to compare the safety and effectiveness of the Altis Single Incision Sling (SIS) to an FDA cleared transobturator and/or retropubic sling through 36 months.

NCT ID: NCT02342678 Completed - Clinical trials for Urinary Incontinence

Lessening Incontinence Through Low-impact Activity

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

The LILA study is a pilot randomized parallel-group trial of a group-based yoga therapy program versus physical conditionin control program for treatment of urinary incontinence in ambulatory middle-aged and older women. Women aged 50 years and older who meet the criteria for frequency of incontinence episodes, are not using other clinical treatments for incontinence, and meet minimum physical mobility requirements and other eligibility criteria will be recruited from the general San Francisco Bay Area.

NCT ID: NCT02338726 Completed - Quality of Life Clinical Trials

Pelvic Floor Symptoms and Quality of Life in Elderly Women - a Population-based Pilot Study

Start date: September 2015
Phase: N/A
Study type: Observational

To assess pelvic floor symptoms and quality of life in elderly women.

NCT ID: NCT02334878 Completed - Clinical trials for Urinary Incontinence, Stress

Stem Cell Therapy for Treatment of Female Stress Urinary Incontinence

Start date: October 1, 2015
Phase: Phase 3
Study type: Interventional

This study evaluates the effectiveness of mesenchymal stem cells in treatment of stress urinary incontinence due to intrinsic sphincter deficiency; in which the problem is weakness or damage of the sphincter muscle responsible for continence. Mesenchymal stem cells are undifferentiated cells which can undergo self-renewal & differentiation into other cell types like muscle cells; thus can be used to regenerate the damaged sphincter muscles. In this study mesenchymal stem cells will be obtained from bone marrow from the patient, processed, & then re-injected periurethrally. Effectiveness will be compared to that of the surgical treatment (tension-free vaginal tape).

NCT ID: NCT02328092 Completed - Nocturnal Enuresis Clinical Trials

A Double-blind Randomized Clinical Trial on the Efficacy of Magnetic Sacral Roots Stimulation for the Treatment of NE

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

The purpose of this study is to assess the efficacy of daily sacral root magnetic stimulation for 10 sessions in patients with nocturnal enuresis.Eligible patients were randomized to receive either real or sham repetitive sacral root magnetic stimulation (rSMS; 15 Hz with a total of 1500 pulses/session) for 10 sessions. Evaluation was performed before starting treatment, immediately after the 5th and 10th treatment session, and 1 month later, using frequency of enuresis/week, visual analogue scale (VAS) and Quality of life. Cortical excitability of upper and lower limbs were done before and after the end of sessions.

NCT ID: NCT02319096 Completed - Clinical trials for Urinary Stress Incontinence

Vibration Training and Pelvic Floor Muscle Strength in Females With Stress Urinary Incontinence

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

Pelvic floor muscle training (PFMT) is the first line therapy recommended by NICE for the treatment of SUI. Due to poor motivation and compliance only 15-20% of women comply with the regimen. Whole body vibration (WBV) exercise has been developed as a new modality in the field of physiotherapy. The Galileo machine is a unique device for applying whole-body vibration. The investigators are currently using this therapy as an alternative to traditional pelvic floor muscle therapy. The investigators aim to audit the investigators treatment of whole body vibration.