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Urinary Incontinence clinical trials

View clinical trials related to Urinary Incontinence.

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NCT ID: NCT00329862 Terminated - Hypertension Clinical Trials

Laparoscopic Adjustable Gastric Banding With Truncal Vagotomy

Start date: May 2006
Phase: N/A
Study type: Interventional

Laparoscopic Adjustable Gastric Banding (LAGB) is a gold standard in the surgical treatment of morbid obesity. We hypothesize that the addition of truncal vagotomy (cutting of nerves to the stomach) will produce greater weight loss and better reduction of co-morbidities (diseases caused by or aggravated by morbid obesity) than LAGB alone. 25 patients will be enrolled and outcomes compared to LAGB historical controls over a post-operative period of 24 months.

NCT ID: NCT00323635 Terminated - Clinical trials for Urinary Incontinence

A Comparison of Tolterodine and Placebo Treatments on Nocturnal Frequency and Sleep Quality in Women After Menopause.

Start date: April 2006
Phase: Phase 4
Study type: Interventional

This study is being done to compare frequency of urination during the night when women take tolterodine tablets vs. when they take placebo tablets. We will also measure whether between these two treatment conditions there are any differences in women's sleep, mood and performance on cognitive tests.

NCT ID: NCT00258037 Terminated - Stroke Clinical Trials

Effect of Pelvic Floor Muscle Training in Stroke

Start date: January 1999
Phase: Phase 2
Study type: Interventional

Aim: To evaluate the long term effect of pelvic floor muscle training in women with urinary incontinence after ischemic stroke measured by quality of life paramters.

NCT ID: NCT00253006 Terminated - Clinical trials for Urinary Incontinence

Analysis of Expression of Nitric Oxide Syntheses and Their Functional Role in Human Urothelium

Start date: January 2006
Phase: N/A
Study type: Observational

Painful bladder syndrome (PBS)/interstitial cystitis (IC) may be due to the actions of nitric oxide (NO) in the bladder tissue. NO is a gaseous substance with a very short half-life, synthesized by a group of NO-synthase-enzymes in many tissues. The goal of this study is to illuminate bladder tissue production of NO in individuals with PBS and healthy individuals, by quantification of NO and NO-enzyme expression by different molecular biological methods.

NCT ID: NCT00247286 Terminated - Clinical trials for Urinary Incontinence, Stress

Weighted Vaginal Cones Versus Biofeedback in the Treatment of Urodynamic Stress Incontinence: a Randomized Trial.

Start date: September 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the objective (urodynamic) cure rates and effect on patient quality of life after six months of treatment for two different nonsurgical management options for genuine stress urinary incontinence in females: weighted vaginal cones and formal supervised pelvic floor physiotherapy with biofeedback. Hypothesis: Assuming a minimum of six months of treatment, weighted vaginal cones are as effective as a formal supervised program of pelvic floor physiotherapy with biofeedback for the treatment of uncomplicated genuine stress urinary incontinence in females.

NCT ID: NCT00178282 Terminated - Clinical trials for Urinary Incontinence

Low-Intensity Physical Therapy for Prevention of Pre and Postpartum Urinary Incontinence

Start date: June 2005
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if pelvic exercises can reduce the occurrence of urinary incontinence (involuntary loss of urine) before and after delivery. We would also like to see if performing pelvic exercises before birth has an effect on labor and/or delivery, and if there are any specific characteristics for developing urinary incontinence during pregnancy and after delivery.

NCT ID: NCT00099372 Terminated - Clinical trials for Urinary Incontinence

Long-term Effectiveness of Abdominal Sacrocolpopexy for the Treatment of Pelvic Organ Prolapse

E-CARE
Start date: May 2004
Phase:
Study type: Observational

The Colpopexy and Urinary Reduction Effort (CARE) trial is a research study designed to evaluate whether the addition of a second surgical procedure in addition to a procedure for female pelvic organ prolapse (POP) affects the rates of urinary incontinence. This study will follow women in the CARE study for 10 years from the time of the surgery to compare success and complication rates in the two groups. Recruitment into this study is open only to women that already participated in CARE. Recruitment into CARE is closed.

NCT ID: NCT00084110 Terminated - Hypertension Clinical Trials

Use of Complementary and Alternative Medicine Among Older Mexican Americans

Start date: August 1993
Phase: N/A
Study type: Observational

The purpose of this study is to examine complementary and alternative medicine use among older Mexican Americans and to determine how this use influences physical, functional, and mental health.