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Overactive Bladder clinical trials

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NCT ID: NCT02377765 Completed - Overactive Bladder Clinical Trials

Use of Transcutaneous Posterior Tibial Nerve Stimulation (TPTNS) in Maintaining OAB Symptoms Improvement.

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

This study will help to determine the effectiveness of a self-supervised, home-based Transcutaneous Posterior Tibial Nerve Stimulation treatment protocol in maintaining Overactive Bladder (OAB) symptoms improvement in women responders to Posterior Tibial Nerve Stimulation (PTNS)

NCT ID: NCT02361502 Recruiting - Overactive Bladder Clinical Trials

MIrabegron With oveRACtive bLadder Symptoms in mEn

Start date: February 2015
Phase: Phase 4
Study type: Interventional

The proportion of male patients who participated in the phase III study of mirabegron was about 28% and the data on the efficacy and safety of mirabegron in Korean male OAB patients have limits. For this reason, this study will assess the efficacy and safety of mirabegron in Korean male OAB patients.

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: NCT02327936 Completed - Overactive Bladder Clinical Trials

Fesoterodine and Oxybutynin XL for Overactive Bladder Syndrome in Children

FOXY
Start date: December 2014
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the tolerability of Fesoterodine and Oxytbutynin XL and to compare their efficacy for overactive bladder syndrome in children.

NCT ID: NCT02320773 Completed - Overactive Bladder Clinical Trials

A Prospective Non-interventional Study in Overactive Bladder (OAB) Patients Prescribed Betmiga® as Part of Routine Clinical Practice

BELIEVE
Start date: November 25, 2014
Phase:
Study type: Observational

A study to understand the impact of Betmiga® on patients quality of life, satisfaction with treatment, how long patients remain on treatment, patterns of healthcare resource utilisation, and safety as prescribed by the physicians in routine clinical practice.

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: 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: 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: NCT02279615 Not yet recruiting - Overactive Bladder Clinical Trials

Efficacy And Safety Of Combination Therapy For Treatment Of Overactive Bladder In Male Patients With Benign Prostatic Hyperplasia.

Start date: December 2021
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate the safety and efficacy of combination therapy involving β3-adrenoceptor agonist, mirabegron, and α-blockers for the treatment of OAB symptoms in male patients with BPH.

NCT ID: NCT02271607 Completed - Overactive Bladder Clinical Trials

The Effect and Safety of Moxibustion Therapy for Overactive Bladder Patients

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

This pragmatic randomized controlled study aimed to evaluate the effectiveness and safety of moxibustion therapy on overactive bladder (OAB) patients.