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Overactive Detrusor clinical trials

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NCT ID: NCT04270526 Completed - Overactive Bladder Clinical Trials

Minimizing Pain During Office Intradetrussor Botox Injection

Start date: August 15, 2020
Phase: Phase 4
Study type: Interventional

This will be a prospective double-blinded randomized controlled trial comparing two pre-treatment protocols for patients undergoing intradetrussor botox injections to determine if a buffered lidocaine solution offers superior pain control.

NCT ID: NCT04197466 Completed - Overactive Bladder Clinical Trials

Comparison of Different Treatments for Overactive Bladder Syndrome

Start date: December 6, 2019
Phase: N/A
Study type: Interventional

This study aims to investigate the effects of pelvic floor muscle exercises, electrical stimulation and taping in patients with overactive bladder

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: 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: NCT02657057 Completed - Overactive Bladder Clinical Trials

Effects of Transcutaneous and Percutaneous PTNS on Idiopathic OAB

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

The purpose of this study is to determine if Transcutaneous Tibial Nerve Stimulation (TENS) is as effective as Percutaneous Tibial Nerve Stimulation (PTNS) as therapeutic option for subjects with Idiopathic Overactive Bladder (OAB) who have failed conventional therapy.

NCT ID: NCT01837654 Completed - Overactive Detrusor Clinical Trials

Plantarflexion Reduces Urgency and Peak Detrusor Pressure in Patients With Detrusor Overactivity

DO
Start date: June 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to find out whether plantarflexion has an effect on the degree of urinary urgency and on the amplitude of detrusor contraction during filling cystometry in patients with detrusor overactivity (DO).

NCT ID: NCT01781117 Completed - Overactive Detrusor Clinical Trials

Prognostic Value of the Urinary Nerve Growth Factor in the Patients With Benign Prostatic Hyperplasia

Start date: February 2013
Phase: N/A
Study type: Interventional

Persistent detrusor overactivity (DO) after transurethral prostatectomy results in symptomatic failure in more than one third of the patients. Storage symptoms are major complaints in the early postoperative period after Holmium Laser Enucleation of the Prostate (HoLEP). Levels of the urinary nerve growth factor (NGF), produced by bladder urothelium and smooth muscle, are increased in the patients with overactive bladder (OAB), and decreased after the OAB symptoms were improved. Also, urinary NGF levels are increased in patients with benign prostatic obstruction (BPO), but the changes of the NGF levels after relief of the BPO by the medical or surgical treatment have not been fully investigated. If the elevated urinary NGF levels are reduced after successful surgical treatment of BPO, measurement of urinary NGF could be a useful objective tool to assess the therapeutic outcomes of the operation. The aims of this study are to measure the urinary NGF levels in patients with BPO and to compare the results between the patients with detrusor overactivity (DO) and without detrusor overactivity (Non-DO), average 2 weeks before Holmium Laser Enucleation of the Prostate (HoLEP) procedure. After HoLEP, urinary NGF levels are rechecked at the periods of postoperative 3 months and 6 months, and compare changes between the two groups.

NCT ID: NCT01629433 Completed - Overactive Detrusor Clinical Trials

Onabotulinumtoxina Intradetrusorial Injections and NGF Expression

Onab/A-NGF
Start date: January 2009
Phase: Phase 4
Study type: Observational

In the last years, botulinum toxin type A (onab/A) has been increasingly used as a treatment option for overactive bladder symptoms in patients affected by either neurogenic and idiopathic detrusor overactivity (DO). How onab/A injected into the detrusor muscle improves overactive bladder symptoms in neurologic patients has been only partially investigated.Some evidence suggested that the neurotoxin probably reduces detrusor muscle contraction blocking detrusor muscle cholinergic innervation. However, recent experimental observations indicated that onab/A determines more complex effects on bladder activity acting on afferent innervations as well as on the efferent one. Only few experimental studies have investigated the activity of onab/A on bladder afferent nervous transmission. Experimental studies in animals showed that Nerve Growth Factor (NGF) elicits increased sensation, urgency and DO. Although there are some evidence on the ability of onab/A to improve DO and to reduce bladder and urinary content of NGF, how onab/A influences NGF expression and the expression of TrKa, p75 and TRPV1 receptors is still unclear. The hypothesis is that onab/A reduces NGF bladder tissue levels and in the same time it modulates the gene expression of NGF associated receptors (TrkA, p75 and TRPV1).

NCT ID: NCT01408771 Completed - Overactive Detrusor Clinical Trials

"Swallow my Urine Back" : Inhibition of Detrusor Overactivity by Swallowing Maneuver

Start date: April 2011
Phase: N/A
Study type: Observational

The purpose of this study is to find out whether swallowing has an effect on the degree of urinary urgency and on the amplitude of detrusor contraction during filling cystometry in patients with detrusor overactivity (DO).

NCT ID: NCT01192568 Completed - Neurogenic Bladder Clinical Trials

Safety and Efficacy Evaluation of Oxybutynin Topical Gel In Children With Neurogenic Bladder

Start date: May 2, 2011
Phase: Phase 4
Study type: Interventional

This study will evaluate the safety and efficacy of Oxybutynin Chloride 10% Topical Gel in children 3 to less than 17 years old, who have overactive bladder due to a neurogenic condition. Children will be treated with 0.75 g of gel/day for two weeks. Patients will then return to the clinic for a potential dose titration. At this time their dose may be adjusted up to 1g/day, down to 0.5g/day, or remain the same at 0.75g of gel/day depending on the individual response and tolerability. The total treatment time is 14 weeks and total time on the study is 16 weeks.