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Incontinence clinical trials

View clinical trials related to Incontinence.

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NCT ID: NCT02835846 Completed - Overactive Bladder Clinical Trials

Investigation of the Effect of the Female Urinary Microbiome on Incontinence

FUM
Start date: September 2016
Phase: Phase 4
Study type: Interventional

This purpose of this study is to understand the types of bacteria that are in the bladder and vagina in patients with overactive bladder (OAB) symptoms and understand if the types of bacteria change when with the use of estrogen in the vagina. The investigators are also trying to understand how estrogen influences the body's ability to make substances called peptides that can kill bacteria.

NCT ID: NCT02633592 Completed - Incontinence Clinical Trials

Seated Evaluation of Anorectal funcTion by High Resolution Anorectal Manometry

SEAT
Start date: November 2014
Phase: N/A
Study type: Interventional

To assess whether HR-ARM (High resolution Anorectal Manometry) performed in the more naturalistic / physiological upright, seated position on a commode provides a more valid assessment of anorectal function and simulated defecation than the same test performed in the standard, left lateral position

NCT ID: NCT02616081 Completed - Quality of Life Clinical Trials

Patient Reported Outcomes for Bladder Management Strategies in Spinal Cord Injury

NBRG-PCORI
Start date: January 1, 2016
Phase:
Study type: Observational

The investigators goal is to create a better understanding of patient reported outcomes for bladder management strategies (clean intermittent catheterization (CIC), indwelling catheter (IDC) and bladder surgery.

NCT ID: NCT02554201 Completed - Clinical trials for Spinal Cord Injuries

Efficacy of Electrical Pudendal Nerve Stimulation for Neurogenic Lower Urinary Tract Dysfunction

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

The main goal to treat early NLUTS is to relieve lower urinary tract syndrome and prevent from late complications. The present study is to evaluate the efficacy of electrical pudendal nerve stimulation (EPNS) and transanal/transvaginal electrical stimulation (TES) in NLUTD.The study design consists of a non-randomized, parallel controlled trial. A total of 60 eligible patients will be involved and divided into EPNS or TES group according to their location of medical treatment. The primary endpoint is lower urinary tract syndromes (ICIQ-FLUTS/MLUTS). The second endpoint is assessment of daily life Qol (ICIQ-LUTSqol), and residual urine volume.

NCT ID: NCT02168556 Completed - Incontinence Clinical Trials

Interventions to Decrease Anxiety in Patients Undergoing Urodynamic Testing

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

This is a randomized controlled trial to determine if music, a video, or standard of care will decrease anxiety in patients undergoing urodynamic testing.

NCT ID: NCT02136693 Completed - Constipation Clinical Trials

Psyllium Fiber Versus Placebo in Early Treatment After STARR for Obstructed Defecation: a Double-blind RCT

Start date: May 2010
Phase: Phase 4
Study type: Interventional

This study aims to assess whether fiber intake, formerly recommended only before or instead of surgery, may play a role in improving postoperative progress and functional outcome after STARR for obstructed defecation, in terms of residual constipation, incontinence and defecation urgency.

NCT ID: NCT01978210 Completed - Autism Clinical Trials

Development of a Manualized Wireless Moisture Pager Intervention for Teaching Toileting in Children With Autism

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

This pilot study is designed to investigate the feasibility of comparing a standard behavioral intervention and an innovative intervention that incorporates the use of a wireless moisture alarm in training children with autism how to independently use the toilet for urination. We hypothesize that the study protocol will be feasible, as measured through review of achieved recruitment targets, successful randomization, and >80% retention of subjects with com- plete data collection. Our second hypothesis is that therapists will deliver experimental and standard behavioral treatment intervention with ≥80% fidelity and parents in both intervention groups will adhere to the intervention with ≥80% fidelity. A secondary aim of this study is to examine trends in outcome data by conducting a small RCT (N = 30) of wireless moisture alarm and standard behavioral toilet training, with the hypothesis that the moisture alarm intervention will result in fewer toileting accidents, a higher rate of toileting success and greater parental satisfaction.

NCT ID: NCT01920035 Completed - Incontinence Clinical Trials

Study of Endorectal Cooling During RARP to Minimize Trauma and Promote Earlier Return to Continence

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

Localized cooling/hypothermia using the UroCool System during robotic-assisted radical prostatectomy (RARP) surgery results in an improved overall return to continence, (defined as not wearing any protective urinary pads), compared with standard of care in men presenting for RARP.

NCT ID: NCT01747343 Completed - Incontinence Clinical Trials

Toilet Training Toddlers and Preschoolers

Start date: November 2012
Phase: N/A
Study type: Interventional

The investigators are interested in determining those procedures that prove to be most efficient and effective in facilitating continence (i.e., "dry pants" or the absence of soiled undergarments), appropriate eliminations (i.e., voids/stools in toilet), and independent requests/initiations to use the toilet. To assess the effectiveness of toilet training methods (procedures), data on toileting skills (in addition to each skill in a given child's curriculum) are collected across the school day (7:30 am-5:45 pm) by the classroom teachers. The primary dependent variables (toileting skills) are continence (i.e., absence of soiled undergarments), appropriate eliminations (i.e., the number of voids/stools made in the toilet), and independent/self requests (i.e., communication by the child with an adult to use the toilet). The toileting procedures are implemented by classroom teachers (undergraduate practicum students) and implementation is monitored by classroom supervisors (graduate teaching assistants). Procedural effectiveness is evaluated on a daily basis by the graduate teaching assistants and on an at-least-weekly basis by faculty supervisors.

NCT ID: NCT01523288 Completed - Constipation Clinical Trials

The Intestinal Function in People With Prader-Willi Syndrome

Start date: February 2011
Phase: N/A
Study type: Observational

The projects aim is to investigate the intestinal function of patients suffering from Prader-Willi Syndrome. The methods used are ultrasonographic measurement of the rectal diameter and gastrointestinal transit time