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Urinary Bladder, Overactive clinical trials

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NCT ID: NCT03451175 Completed - Multiple Sclerosis Clinical Trials

Reproductibility of Cystometry in Multiple Sclerosis Patient

Start date: July 2, 2017
Phase: N/A
Study type: Observational

This study evaluates the reproductibility (quantitative and qualitative) of cystometry in mutiple sclerosis patients.

NCT ID: NCT03390790 Completed - Clinical trials for Urinary Incontinence

Lidocaine for Pain After Urodynamic Testing

Start date: January 25, 2018
Phase: Phase 4
Study type: Interventional

Urodynamic testing can be associated with mild discomfort, particularly at the time of insertion, repositioning, and removal of the bladder catheter (a tube inserted into the bladder via the urethra). Few studies have investigated ways to improve patient comfort during this procedure. In this study, the investigators want to see if applying external lidocaine (a numbing gel) prior to the procedure can help to minimize patient discomfort.

NCT ID: NCT03388086 Completed - Neurogenic Bladder Clinical Trials

Efficacy of Two Onabotulinum Toxin Doses

Start date: February 1, 2018
Phase:
Study type: Observational

The changes in bladder function after the injection of Onabotulinum toxin into the detrusor in individuals with neurogenic bladder overactivity will be investigated retrospectively. The records of all patients treated with Onabotulinum toxin injections into the detrusor since 2000 will be evaluated. The changes in the urodynamic values after the injection of 300 units of Onabotulinum toxin will be compared with the changes after the injection of 200 units. Furthermore, the differences in urinary continence, duration between injections, side effects and complications between the two groups will be investigated.

NCT ID: NCT03371342 Completed - Overactive Bladder Clinical Trials

Treatment of MEDITOXIN® in Female Patients With Idiopathic Overactive Bladder

Start date: December 13, 2017
Phase: Phase 1
Study type: Interventional

To investigate the safety of MEDITOXIN in female subjects with idiopathic overactive bladder compared with BOTOX

NCT ID: NCT03320850 Completed - Clinical trials for Urinary Incontinence

BOTOX® Intravesical Instillation in Participants With Overactive Bladder and Urinary Incontinence

APOLLO
Start date: October 4, 2017
Phase: Phase 2
Study type: Interventional

This study will evaluate the efficacy and safety of BOTOX® intravesical instillation in participants with overactive bladder and urinary incontinence.

NCT ID: NCT03280654 Completed - Clinical trials for Visceral Adiposity Index

Visceral Adiposity Index and Overactive Bladder

Start date: January 1, 2015
Phase: N/A
Study type: Observational [Patient Registry]

In present study, we aimed to investigate the association between visceral adiposity index and overactive bladder symptoms in female patients aged over 18 years.Between January-2015 and July-2017, 151 female patient with overactive bladder symptoms were evaluated in Recep Tayyip Erdogan University Training and Research Hospital Urology Department. Antropometric and laboratory features including serum lipid levels, AST, ALT, fasting glucose levels, and also urodynamic findings were recorded. Visceral adiposity index was calculated according to gender-specific formula. Participants were divided into two groups according to 7,55 cut-off level for visceral adiposity index levels. Statistical significance were discussed between two groups.

NCT ID: NCT03250650 Completed - Clinical trials for Overactive Bladder Syndrome

Physiotherapy in Overactive Bladder: Electrical Stimulation Treatment

OAB
Start date: March 9, 2017
Phase: N/A
Study type: Interventional

To evaluate the efficacy of combined transvaginal electrical stimulation (ES) and transcutaneous tibial nerve electrical stimulation (TTNS) in the treatment of female overactive bladder syndrome (OAB).

NCT ID: NCT03175029 Completed - Overactive Bladder Clinical Trials

Exploratory Study of TAC-302 in Detrusor Underactivity Patients With Overactive Bladder.

Start date: August 1, 2017
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of TAC-302 in detrusor underactivity patients with overactive bladder.

NCT ID: NCT03149809 Completed - Parkinson Disease Clinical Trials

Behavioral or Solifenacin Therapy for Urinary Symptoms in Parkinson Disease

BOSS PD
Start date: March 1, 2018
Phase: Phase 3
Study type: Interventional

The impact of urinary symptoms in Parkinson disease (PD) extends beyond worsened well-being. Urinary symptoms common in PD, especially incontinence and nocturia, are major risk factors for falls likely due to the combination of urinary urgency and impaired mobility (and falls are a leading cause of mortality in PD), for spouse/caregiver stress due to decreased mutuality in the relationship, and for institutionalization, largely due to increased disability. Additionally, most medications currently recommended for urinary symptoms in PD are anticholinergic and have the potential to worsen the progressive cognitive and autonomic burdens of the disease. Veterans with PD are also more likely to rely solely on VA for their health care than Veterans without PD. Thus, optimizing the care of urinary symptoms for Veterans with PD becomes imperative, particularly for VA. Using a non-inferiority design, this proposal seeks to demonstrate the comparative effectiveness of pelvic floor muscle exercise-based behavioral therapy versus drug therapy to treat urinary symptoms in PD.

NCT ID: NCT03109379 Completed - Clinical trials for Idiopathic Overactive Bladder With Urinary Incontinence

Safety and Tolerability of TAR-302-5018 in Subjects With Idiopathic Overactive Bladder

Start date: April 4, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if TAR-302-5018, an investigational drug-delivery system, is safe and tolerable in patients with idiopathic overactive bladder and urinary incontinence.