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Urinary Bladder, Overactive clinical trials

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NCT ID: NCT02335853 Recruiting - Overactive Bladder Clinical Trials

Association Between Metabolic Syndrome and Serum Nerve Growth Factor Levels in Women With Overactive Bladder

NGF
Start date: January 2015
Phase: N/A
Study type: Observational

Nerve growth factor (NGF-R) receptors are between the detrusor muscle fibers and can cause afferent signals. Metabolic syndrome and obesity have been advocated to be risk factors for the development of overactive bladder.

NCT ID: NCT02315950 Recruiting - Overactive Bladder Clinical Trials

The Use of cineMRI to Evaluate Botox in Patients With Medication Refractory Overactive Bladder

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

With the goal of providing improved treatment to patients with overactive bladder symptoms (OAB), the investigators seek to apply the new technology of time-resolved (cine) MRI combined with urodynamics (UDS) to understand the exact effect of intravesical botulinum toxin on bladder physiology. The investigators will specifically aim to assess the physiological mechanism by which intravesical botulinum alleviates urgency and urge incontinence symptoms in women with OAB refractory to medical therapy.

NCT ID: NCT02086058 Recruiting - Overactive Bladder Clinical Trials

Gene Expression in the Overactive Bladder in Children

Start date: November 2013
Phase: N/A
Study type: Observational

The aim of this study (the hypothesis) is to identify differences in the gene expression profile in the bladder muscle and hereby gain greater knowledge about the muscular mechanisms that cause overactive bladder and daytime urinary incontinence in children older than 5 years. A secondary aim is to examine how this gene expression profile differs from children with a neurogenic overactive bladder and how the gene expression profile changes from childhood till adulthood. Such new knowledge will result in a more precisely targeted and hence effective treatment of overactive bladder. The results will be obtained by retrieving bladder biopsies from children and adults suffering from an overactive bladder or a neurogenic bladder. These biopsies will undergo molecular analysis and the investigators will compare them with biopises from bladder healthy adults and children.

NCT ID: NCT01876186 Recruiting - Clinical trials for Overactive Bladder Syndrome

Comparisons of 3-month Versus 6-month Solifenacin Treatment for Female OAB Patients

Start date: May 2013
Phase: Phase 4
Study type: Interventional

To investigate whether prolonged period of treatment (6 months) can have a better therapeutic outcome than conventional period (3 months) of antimuscarinics.

NCT ID: NCT01842685 Recruiting - Overactive Bladder Clinical Trials

Bladder Thermal Distention for Patients With Refractory Overactive Bladder

OAB
Start date: April 2013
Phase: N/A
Study type: Interventional

In this study, the investigators will evaluate the efficacy of Bladder Thermal Distention (BTD) in patients with overactive bladder syndrome who failed previous treatment of anticholinergic drugs. The investigators' hypothesis is that it will improve the storage symptoms.

NCT ID: NCT01640002 Recruiting - Clinical trials for Overactive Bladder Associated With HTLV-1

A Randomized, Placebo-Controlled Study to Assess the Efficacy of Propantheline for the Treatment of Overactive Bladder

Start date: May 2012
Phase: Phase 1
Study type: Interventional

It's a double blind, placebo controlled study to assess the efficacy of Propantheline Bromide to treat overactive bladder (OAB) in HTLV 1 infected patients. We think that the treatment of the OAB with Propantheline could reduce nocturia and frequency in sixty percent.

NCT ID: NCT01627145 Recruiting - Clinical trials for Overactive Bladder Syndrome

Post-treatment Novmalized Urodynamiz Findings as the Golden Standard of Objective Cure for Female Overactive Bladder Patients Receiving Antimuscarinic Drug

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

Post-treatment Novmalized Urodynamiz Findings as the Golden Standard of Objective Cure for Female Overactive Bladder Patients Receiving Antimuscarinic Drug and Its Conelations With Voiding Diary, King's Health Quentionaire, Overactive Bladder Sympton Scores and Patient Perception of Bladder Condition.

NCT ID: NCT01613170 Recruiting - Overactive Bladder Clinical Trials

Premarin Versus Toviaz for Treatment of Overactive Bladder

Start date: April 2012
Phase: Phase 4
Study type: Interventional

The use of vaginal estrogen cream in conjunction with Toviaz will be more effective than the use of Toviaz alone for the treatment of overactive bladder.

NCT ID: NCT01595152 Recruiting - Clinical trials for Urinary Bladder, Overactive

Solifenacin Succinate Versus Fesoterodine A Comparison Trial for Urgency Symptoms

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

Hypothesis: Objective 1: To advance the investigators understanding on the effect of solifenacin succinate (10 mg OD) vs. fesoterodine (8mg OD) on urinary urgency using a validated Urgency Severity and Impact Questionnaire (USIQ). Hypothesis 1.1: The severity of urgency symptoms as measured by USIQ will change differently in women with OAB following a 3 month treatment with solifenacin succinate (10 mg OD) vs. fesoterodine (8mg OD). Hypothesis 2.1: Condition-specific quality of life (QOL) as measured by USIQ will change differently in women with OAB following a 3 month treatment with solifenacin succinate (10 mg OD) vs. fesoterodine (8mg OD). Objective 2: To advance the investigators understanding on the adverse events (AE's) of solifenacin succinate (10 mg OD) vs. fesoterodine (8mg OD). Hypothesis 1.1: The severity and rate of AE's in women with OAB following a 3 month of treatment with solifenacin succinate (10 mg OD) vs. fesoterodine (8mg OD) will be different.

NCT ID: NCT01569061 Recruiting - Overactive Bladder Clinical Trials

Painless Laser Therapy for Overactive Bladder

PLTOAB
Start date: February 2012
Phase: N/A
Study type: Interventional

The primary objective of this study is to determine the effectiveness of transvaginally-delivered low level laser therapy (LLLT) versus Sham in the treatment of overactive bladder symptoms in women. The secondary objective is to determine the effect of transvaginally-delivered LLLT vs. sham on the quality of life.