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Overactive Bladder clinical trials

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NCT ID: NCT02110680 Withdrawn - Overactive Bladder Clinical Trials

Efficacy of Transcutaneous Nerve Stimulation on Improvement of Overactive Bladder Symptoms

TENSOAB
Start date: March 2016
Phase: Phase 2
Study type: Interventional

Overactive bladder (OAB) is a very common problem that impairs the quality of life of about 17% of adult population in USA above the age of 40. The issues becomes more prominent with getting older. OAB was determined by International Continence Society as urgency (immediate desire to urinate that could not be postponed) with or without incontinence usually associated with increased frequency and nocturia (urination at night). In 2012, American Urologic Association published clinical guidelines for the treatment of OAB of non neurogenic origin. Neuromodulation was proposed as the third line of treatment and two treatments were recommended: sacral nerve neuromodulation (SNM) and posterior tibial nerve stimulation (PTNS). Each of above mentioned procedures are invasive. SNM involves lead implantation in operating room using X-ray guidance and anesthesia. PTNS involves needle insertion on the low extremity. The investigators would like to examine the efficacy of transcutaneous nerve stimulation (TENS) in refractory to the first two lines of OAB treatment patients.

NCT ID: NCT01210859 Withdrawn - Overactive Bladder Clinical Trials

Effects of Antimuscarinic Drugs on Overactive Bladder (OAB) Symptoms After Insertion of Ureteral Stents

Start date: September 2010
Phase: N/A
Study type: Observational

The purpose of this study is to check whether antimuscarinics that usually broadly used in the treatment of overactive bladder symptoms are effective in the treatment of those symptoms after insertion of ureteral stents. In order to study the efficacy of the treatment of OAB symptoms in stented patients the investigator will use a suitable questionnary.

NCT ID: NCT01003405 Withdrawn - Overactive Bladder Clinical Trials

Long-term Safety and Efficacy of KUC-7483 in Patients With Overactive Bladder

Start date: n/a
Phase: Phase 3
Study type: Interventional

To investigate the long-term safety, efficacy and pharmacokinetics of KUC-7483 in patients with overactive bladder.

NCT ID: NCT00773552 Withdrawn - Overactive Bladder Clinical Trials

Solifenacin Succinate Versus Placebo in Inner City Women Ages 20-45 With Overactive Bladder

Start date: November 2008
Phase: Phase 4
Study type: Interventional

In this study we hope to establish the prevalence of urinary urge symptoms (with or without incontinence) in a multicultural, underserved, hospital clinic population in women between the ages of 20 and 45. Quality of life (QOL) in these individuals will be examined. The goal is to show a 15% reduction in number of voids in a 24 hour period in our study population after 12 weeks of treatment with solifenacin succinate. Hypothesis: We believe that urinary urge symptoms are under-reported in young women and believe they pose a significant strain on quality of life on otherwise young, healthy individuals. Treatment with solifenacin succinate will improve symptoms, in turn improving QOL for these individuals.

NCT ID: NCT00594139 Withdrawn - Overactive Bladder Clinical Trials

Autologous Neo-Bladder Construct in Non-Neurogenic Overactive Bladder and Urge Predominant Incontinence

Start date: January 2008
Phase: Phase 2
Study type: Interventional

Subjects with non-neurogenic over-active bladder will be enrolled. The hypothesis is that augmentation cystoplasty using an autologous neo-bladder construct will increase functional capacity and thereby reduce the number of micturition episodes per day in subjects with non-neurogenic over active bladder and urge predominant incontinence.

NCT ID: NCT00262496 Withdrawn - Clinical trials for Urinary Incontinence

Botulinum-A Toxin Injection for Detrusor Hyperreflexia in Spinal Cord Injury: A Non-Surgical Approach.

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of the study is to determine whether Botulinum-A toxin injected in the bladder muscle will help prevent the frequency and degree of urinary incontinence in Spinal Cord Injured and Multiple Sclerosis patients. The proposed mechanism would be that the Toxin would allow the bladder to hold more urine at a lower pressure as determined by Urodynamics. The research will answer the question whether the dosages 300 units vs 400 units are either equally vs not equally effective in helping urinary incontinece and bladder storage.