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Active clinical trials for "Urinary Bladder, Overactive"

Results 471-480 of 730

Developing a Simple Test to Diagnose Overactive Bladder

Overactive BladderOveractive Bladder Syndrome1 more

In order to develop a test to diagnose overactive bladder from urine, it is essential that this test is at least as accurate as the tools that clinicians currently use. As such, this study will compare the performance of the device in development to the performance of existing methods.

Not yet recruiting8 enrollment criteria

Virtual Reality (VR) During Peripheral Nerve Evaluation (PNE) Procedure

Overactive Bladder

The purpose of this research is to evaluate whether or not wearing a virtual reality headset affects pain and anxiety in patients undergoing percutaneous nerve evaluation (PNE).

Withdrawn3 enrollment criteria

Tetra-NIRS Clinical Study

Lower Urinary Tract SymptomsOveractive Bladder

The purpose of this evaluation is to validate the previous clinical study results using a Near-Infrared Spectroscopy (NIRS) device, as compared to the conventional urodynamics (UDS) testing. The experiment will use the commercially available Tetra-NIRS and Laborie UDS equipment. The hypothesis is that the Tetra-NIRS device, in the clinical environment, provides data to enhance the analysis using the standard urodynamics equipment (stand-alone Urodynamic procedure).

Terminated7 enrollment criteria

FemPulse Therapy First-in-Human Experience

Urinary BladderOveractive

The purpose of this clinical trial is to investigate a new medical device treatment for Overactive Bladder (OAB) in women.

Completed8 enrollment criteria

Supraspinal Control of Lower Urinary Tract Function in Healthy Controls and Patients With Bladder...

Neurogenic Lower Urinary Tract DysfunctionMultiple Sclerosis2 more

The purpose of this study is to provide profound insight into the supraspinal neuronal mechanisms and networks responsible for lower urinary tract (LUT) control and to verify, amend or adjust neuronal circuitry models established from findings in healthy subjects in the context of neurogenic and non-neurogenic LUT dysfunction.

Completed104 enrollment criteria

Single Dose Study to Measure Blood Levels and Safety of a Drug for Children With Overactive Bladder...

Overactive BladderNeurogenic Detrusor Overactivity

The purpose of this study is to evaluate blood levels of solifenacin succinate (the study drug) in children with neurogenic detrusor overactivity after taking a single oral dose. If the bladder contracts strongly and without warning, the muscles surrounding the urethra (detrusor muscles) may not be able to keep urine from passing. This may happen as a consequence of spinal cord defects, and then is called neurogenic detrusor overactivity.

Completed31 enrollment criteria

A Study to Evaluate the Pharmacokinetics, Safety and Tolerability of Mirabegron OCAS (Oral Controlled...

Neurogenic Detrusor OveractivityOveractive Bladder1 more

The purpose of this study is to evaluate the pharmacokinetics as well as the safety and tolerability of mirabegron OCAS tablets after single-dose administration at different dose levels in children and adolescents with NDO or OAB.

Completed54 enrollment criteria

Dose-Escalating Study of Propiverine Hydrochloride in Children Suffering From Overactive Bladder...

Overactive Bladder

The open-label dose-escalating two-centre study was designed to assess the pharmacokinetics as well as safety, tolerability and efficacy parameters of propiverine in patients 5-10 years of age suffering from frequency-urgency-syndrome and urinary incontinence indicative of detrusor overactivity (overactive bladder) for determination of the recommended dose in children.

Completed10 enrollment criteria

A Clinical Study to Determine the Effect of YM178 on the Pharmacokinetics of Warfarin in Healthy...

Overactive BladderPharmacokinetics

This study investigates whether YM178 has an effect on the pharmacokinetics of warfarin, to exclude any drug-drug interaction between YM178 and warfarin, and evaluates the safety and tolerability of warfarin alone and combined with YM178.

Completed12 enrollment criteria

A Parallel Group Study to Compare Sativex® With Placebo in the Treatment of Detrusor Overactivity...

Detrusor OveractivityMultiple Sclerosis

The purpose of this study is to evaluate the efficacy of Sativex® compared with placebo in reducing the daily number of episodes on incontinence.

Completed24 enrollment criteria
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