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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT02139956 Active, not recruiting - Clinical trials for Urinary Incontinence Due to Urethral Sphincter Incompetence

Assessment of the Internal Urethral Sphincter and the Vagina by Three Dimensional Ultrasound

Start date: May 2014
Phase: N/A
Study type: Observational [Patient Registry]

Continent women have an intact internal urethral sphincter that extends from the bladder neck down to the perineal membrane. The internal urethral sphincter is a strong collagen muscle tissue cylinder lined by urothelium. On ultrasound scanning tissue echo will be detected torn internal urethral sphincter will not stand sudden rise of abdominal pressure. Three dimensional ultrasound assessment of the internal urethral sphincter is very sensitive and specific for the diagnosis of stress urinary incontinence.

NCT ID: NCT02039830 Active, not recruiting - Clinical trials for Urinary Incontinence

Group Versus Individual Physiotherapy for Urinary Incontinence in Aging Women

GROUP
Start date: July 2012
Phase: N/A
Study type: Interventional

The recommended treatment for urinary incontinence (UI) in women is individualised pelvic floor muscle (PFM) training, a costly and resource-intense approach; one Canada is currently unable to meet. This non-inferiority randomized control trial seeks to determine if group-based PFM training is as effective as individualised PFM training for treating UI in women 65 and over, and to establish the cost-effectiveness of both. Demonstrating that group-based treatment is at least as good as individualised one-on-one treatment and more cost-effective would warrant including group-based PFM training as a first-line UI treatment.

NCT ID: NCT01933854 Active, not recruiting - Clinical trials for Urinary Incontinence

Urinary Incontinence in Women From Amapa

iuemcp
Start date: February 2013
Phase: N/A
Study type: Observational [Patient Registry]

The investigators aim to study the prevalence of urinary incontinence in women who live in the riverside community in the state of Amapa (The Bailique Island) and compare it to the prevalence of urinary incontinence in women who live in the urban region -Macapa-the capital city of the Amapa State - Brazil.

NCT ID: NCT01648491 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Autologous Stem Cells for Urinary Incontinence: Single Patient Compassionate Use

Start date: March 2011
Phase: N/A
Study type: Interventional

Determine safety and effectiveness of the technique using autologous stem cells in the treatment of urinary incontinence in one male subject.

NCT ID: NCT01599715 Active, not recruiting - Clinical trials for Urinary Incontinence

Translating Unique Learning for Incontinence Prevention

TULIP
Start date: September 2010
Phase: Phase 2
Study type: Interventional

More than one in three US women suffers from the distressing, embarrassing, and often unreported problem of urinary incontinence (UI). UI severity increases with age and the financial cost exceeds $19 billion per year . The Adult Conservative Management Committee of the 2008 International Consultation on Incontinence concluded that pelvic floor muscle training (PFMT) should be offered as first line therapy to all women with stress, urge, or mixed UI; and that bladder training (BT) may be preferred to drug therapy. Conservative strategies are low risk and differ from other forms of UI management in that they do not prejudice future treatments. They also may decrease symptoms of urgency and frequency that do not entail UI, but greatly reduce the quality of life for nearly 1 in 11 US women.

NCT ID: NCT01540656 Active, not recruiting - Clinical trials for Urinary Incontinence

Mechanical Nerve Stimulation in the Treatment of Post Prostatectomy Incontinence

Start date: June 2012
Phase: Phase 3
Study type: Interventional

During transcutaneous mechanical nerve stimulation in spinal cord injured men an increase in pressure was observed in the external urethral sphincter along with an increase in bladder capacity. In a subsequent study it was demonstrated that Transcutaneous Mechanical Nerve Stimulation (TMNS) in women could induce pressure increment of the external urethral sphincter. A pilot study have since shown that after 6 weeks of stimulation 24 out of 33 women suffering from urinary stress incontinence were able to contract their pelvic floor muscles and had become free of symptoms. Another pilot study has shown promising effect on the overactive bladder syndrome. Furthermore pilot studies in men who are incontinent after a radical prostatectomy have shown promising results. A randomized investigation of TMNS applied in the immediate period after a radical prostatectomy to investigate effects on both continence and erectile function is on going. The present study aims to treat urinary incontinence in men who are still incontinent more than 1 year after a radical prostatectomy. A medical vibrator is used daily for a period of 6 weeks and the results of the treatment is then evaluated. The participants will be randomized to 2 groups. Group 1 starts vibration treatment at base line and group 2 starts after 6 weeks when group 1 is done. The groups are compared at baseline, at 6 weeks and at 12 weeks. The stimulation will be performed at the frenulum of the glans penis every day for 6 weeks with an amplitude of 2 mm and a frequency of 100 Hz. Results will be evaluated on the basis of questionnaires, micturition diaries and diaper tests. If the investigators are able to demonstrate a significant reduction in the incontinence symptoms in the subjects the investigators asses that vibration can be a way of reestablishing normal continence in men after a radical prostatectomy.

NCT ID: NCT01323426 Active, not recruiting - Clinical trials for Urinary Incontinence, Stress

Treatment of Stress Urinary Incontinence by Injection of Autologous Muscle Fibers Into the Urethral Sphincter.

Start date: May 2010
Phase: Phase 1/Phase 2
Study type: Interventional

This pilot study examines safety and efficacy of a simple procedure for treatment of stress urinary incontinence. A muscle biopsy is taken from the thigh, minced and injected into the urethral sphincter.

NCT ID: NCT01115465 Active, not recruiting - Clinical trials for Stress Urinary Incontinence

Study of Macroplastique Safety and Effectiveness in the Treatment of Female Stress Urinary Incontinence

ROSE
Start date: January 2008
Phase: N/A
Study type: Interventional

The ROSE Registry will determine the long-term safety and effectiveness of Macroplastique in the treatment of female stress urinary incontinence (SUI) due to intrinsic sphincter deficiency (ISD).

NCT ID: NCT00982098 Active, not recruiting - Clinical trials for Urinary Incontinence

Prevention of Urinary Incontinence After Prostatectomy

Start date: February 2007
Phase: N/A
Study type: Interventional

Urinary incontinence is a frequent complication after radical prostatectomy. Rehabilitative treatments are frequently utilized to reduce incontinence. However, their efficacy has not been completely investigated. In this study the investigators will compare the effect of an early rehabilitation programme (instruction of the patient, pelvic floor muscle training, electrical stimulation and biofeedback) versus instruction of the patient only. The investigators hypothesis is that early rehabilitation programme is more effective than patient's instruction alone in preventing urinary incontinence after radical prostatectomy.

NCT ID: NCT00564044 Active, not recruiting - Clinical trials for Urinary Incontinence

The Immune Reactivity of Biofilms in Vaginal Mesh Erosion.

Start date: August 2007
Phase: N/A
Study type: Interventional

Aging, birth trauma and extensive pelvic surgery are the causes known to cause advanced pelvic organ prolaspe, fecal as well as urinary incontinence. Surgical treatment is the last resort to manage the above-mentioned clinical manifestations of pelvic floor disorders except the subject is too frail to receive operation. In order to improve the outcome of reconstructive pelvic surgery, reinforcement with synthetic mesh or biological material is the modern trend in pelvic repair. Unfortunately no prosthesis including synthetic or biological is ideal because vaginal erosion with mesh extrusion which is the subject of this protocol and other complications were reported continuously. As per the literature, the rate for mesh vaginal extrusion ranged between 2.4 and 17% when polypropylene which is the most popular synthetic material used for the mid-urethral sling or pelvic reconstructive surgery to date. The causes of this complication are still controversial which include rejection, poor quality of tissue, surgical artifact, material of mesh and etc. A prospective controlled study for the investigation of the cause for mesh vaginal erosion was conducted and the results revealed evidences of immune reactivity after mesh implantation, albeit the evidence was not solid (Am J Obstet Gynecol 2004; 191(6): 1868-1874 ). As per the pilot study initially done by us to determine the biofilm-related-infection, we have found bacterial biofilm could adhere to surfaces and interfaces, i.e. bacteria located in the cells just beneath the contacting surfaces in the electron microscopic (EM) analysis. In addition, soon after bacteria infection, proteins in biofilm undergo conformational changes, making them immunogenic and triggers a typical inflammatory response leading to activation of the complement system. Thus, we plan to use CD (clusters of differentiation) antigens - 4, 8, 20, 25, 40, 68 and quantitative analysis of FoxP3 to determine the function of regulatory T cells in the immune response. In addition, bacterial culture and EM analysis of the excised mesh with surrounding vagina tissue will be performed for further analysis of biofilms.