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Overactive Bladder clinical trials

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NCT ID: NCT05928910 Withdrawn - Overactive Bladder Clinical Trials

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

Start date: January 30, 2024
Phase: N/A
Study type: Interventional

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).

NCT ID: NCT05256498 Withdrawn - Overactive Bladder Clinical Trials

AURA 1: Augmenting Urinary Reflex Activity: Study 1

AURA1
Start date: April 2022
Phase: N/A
Study type: Interventional

AURA 1 (Augmenting Urinary Reflex Activity: study 1) is a study that evaluates the electrophysiological responses of pudendal nerve stimulation using short-duration extracorporeal stimulation

NCT ID: NCT03753750 Withdrawn - Overactive Bladder Clinical Trials

Noninvasive Spinal Cord Stimulation for Neurogenic and Idiopathic Overactive Bladder

Start date: March 24, 2020
Phase: N/A
Study type: Interventional

Overactive bladder (OAB) affects 12-30% of the world's population. The accompanying urinary urgency, urinary frequency and incontinence can impair the ability to work, interact in social activities and can result in poor social functioning. Multiple treatment modalities are available for overactive bladder. However, each therapy has drawbacks that limit its application in certain patient populations. For example, oral medications have significant side effects and suffer from poor adherence. Botulinum toxin injection into the bladder wall is invasive, requires re-treatment on a regular basis and carries a risk of urinary retention. Current neuromodulatory techniques are invasive and require highly-specialized care. Therefore, a need exists for a non-invasive, well-tolerated and easily administered therapy for OAB. Transcutaneous spinal cord stimulation (TSCS) has been developed and tested in able bodied individuals to initiate locomotor function as well as in the SCI population for lower extremity and upper extremity function. More recently, we have tested this SCI patients to enable lower urinary tract function and decrease detrusor overactivity, resulting in improved continence.

NCT ID: NCT03087578 Withdrawn - Overactive Bladder Clinical Trials

Comparison of Electroacupuncture to Mirabegron for Treatment of Overactive Bladder

Start date: July 1, 2017
Phase: N/A
Study type: Interventional

This study compares electroacupuncture to mirabegron for treatment of overactive bladder (OAB) symptoms in women who have failed treatment with anticholingeric therapy.

NCT ID: NCT03019094 Withdrawn - Overactive Bladder Clinical Trials

Overactive Bladder Posterior Tibial Implantable MIcro STimulator - 1

OPTIMIST-1
Start date: April 2017
Phase: N/A
Study type: Interventional

Interventional, Prospective, Open Label study

NCT ID: NCT02674269 Withdrawn - Overactive Bladder Clinical Trials

Safety and Efficacy Study of Intravesical Instillations of BotuGelTM, Slow Release RTGel Based Botox® Formulations, in Idiopathic OAB Patients With Urinary Incontinence ("INTIMO2")

INTIMO2
Start date: October 2016
Phase: Phase 1/Phase 2
Study type: Interventional

The study will investigate the safety and efficacy of UroGen's TC-3 Gel for sustained release of Botulinum Toxin A (BTX) in urinary bladder in patients with idiopathic overactive bladder.

NCT ID: NCT02522936 Withdrawn - Overactive Bladder Clinical Trials

Use of Biotene Moisturizing Mouth Spray for Xerostomia Associated With Oral Oxybutynin Use

Start date: August 1, 2018
Phase: Phase 4
Study type: Interventional

This is a randomized placebo controlled trial of the use of Biotene versus no treatment in women receiving oral oxybutynin for overactive bladder. The primary outcome will be rate of discontinuation of oxybutynin at 6 month.

NCT ID: NCT02320201 Withdrawn - Overactive Bladder Clinical Trials

Foot Neuromodulation for Overactive Bladder in Children

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

To determine the effects of electrical stimulation of the nerves in the foot on overactive bladder conditions in children.

NCT ID: NCT02297178 Withdrawn - Clinical trials for Urinary Incontinence

A Follow-net Investigation of a Randomised Study of Cystoscopy and Urethral Dilatation Versus Cystoscopy Alone in Women With Overactive Bladder Syndrome and Impaired Voiding

Start date: August 2016
Phase: N/A
Study type: Observational

Urinary incontinences is a highly prevalent and distressing condition which has a significant impact on health related quality of life in millions of women worldwide. Of all women with incontinence, 90% will have overactive bladder symptoms (OAB), and 50% will have detrusor overactivity (DO) on cystometry. The overactive bladder syndrome is defined by the International Continence society as "Urinary urgency, with or without urge incontinence, usually with frequency and nocturia if there is a no infection or proven pathology" (Abrams et al 2002) Initial management of OAB and DO consists of conservative measures such as altering fluid intake, bladder retraining and drug therapy. The next step consists of interventions such as cystoscopy and urethral dilatation, on the basis that it will allow intrinsic bladder problems such as interstitial cystitis to excluded, excluded, and may confer a symptomatic benefit. The original study showed no benefit of urethral dilatation versus no dilatation at 6 months follow up (Duckett 2007). The investigators do not know the natural history of patients with voiding dysfunction. Therefore reviewing their symptoms will give a better idea of what happens to these patients symptoms over time.

NCT ID: NCT02112786 Withdrawn - Overactive Bladder Clinical Trials

Neuromodulation Implantation Settings Variation for Overactive Bladder

Start date: January 2015
Phase: N/A
Study type: Interventional

Participants receiving neuromodulation treatment for overactive bladder symptoms will be routinely fitted with an impulse generator. However, the setting on the impulse generator will be set to either intermittent or continuous stimulation. Participants will complete voiding logs and surveys for a month. Battery life will be interrogated.After a one week period were the device is turned off, the impulse generator will be turned to the opposite setting (intermittent or continuous) and the one month period will be repeated. Again, voiding logs, surveys, and battery life will be collected. The purpose of this project is to investigate the outcomes of intermittent versus continuous stimulation in patients treated with sacral neuromodulation (SNM) for refractory overactive bladder (OAB) syndrome. In addition, the potential for an improved battery life with intermittent stimulation will be quantified.