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Urinary Bladder, Overactive clinical trials

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NCT ID: NCT04483817 Recruiting - Clinical trials for Overactive Bladder Syndrome

Efficacy of Transcutaneous Versus Percutaneous Posterior Tibial Nerve Stimulation in the Overactive Bladder.

Start date: July 17, 2019
Phase: N/A
Study type: Interventional

The main aim of this study, is compare the effectiveness of transcutaneous posterior tibial nerve stimulation versus percutaneous posterior nerve stimulation in patients with overactive bladder.

NCT ID: NCT04448171 Recruiting - Overactive Bladder Clinical Trials

TENS Used for Pain Management During Office Cystoscopy Botox Injections

Start date: October 28, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to determine how Transcutaneous Electric Nerve Stimulation (TENS) units affects pain management during office cystoscopic Botox injections and patient satisfaction with the procedure .

NCT ID: NCT04444440 Recruiting - Clinical trials for Postoperative Urinary Tract Infection

Antibiotic Prophylaxis for Bladder Botox

Start date: July 6, 2021
Phase: Phase 4
Study type: Interventional

Injection of Botox into the bladder is a common treatment for overactive bladder. Postoperative bladder infection is one of the more frequently reported complications of this procedure. Prophylactic antibiotics given at the time of bladder Botox for the reduction of postoperative bladder infection have not been well studied. The main goal of our study is to determine if prophylactic antibiotics at the time of bladder Botox injection for the treatment of overactive bladder in women reduces postoperative bladder infection. The investigators are proposing a study which will randomize participants into two groups - one receiving Ciprofloxacin and the other receiving placebo pills for three days following the procedure. The primary outcome evaluated will be the difference in postoperative bladder infection between the two groups. The investigators will also investigate differences in reported side effects between the two groups possibly related to antibiotic use. Follow-up will be over six weeks following the procedure.

NCT ID: NCT04429360 Recruiting - Overactive Bladder Clinical Trials

What is the Effect of Prolapse Surgery on Voiding?

PROVOID
Start date: June 8, 2020
Phase:
Study type: Observational

The aim of our study is to examine the effect of prolapse surgery on voiding. Our study is the very first one to combine several innovative low-invasive and low-cost methods to analyse the amelioration or deterioration of voiding function after surgery for pelvic organ prolapse using 3D/4D translabial ultrasound, home-uroflowmetry and patient reported quality of life outcomes.

NCT ID: NCT04364438 Recruiting - Overactive Bladder Clinical Trials

Effectiveness of EMS and TENS in Patients With Overactive Bladder

Start date: March 3, 2020
Phase: N/A
Study type: Interventional

Overactive bladder (OAB) syndrome is a well-recognized set of symptoms which patient experience during the storage phase of the micturition cycle. It is characterized by urgency (a sudden compelling desire to pass urine which is difficult to defer) which, in almost all patients, is accompanied by increased frequency and nocturia and, particularly in female patients, by urgency incontinence.

NCT ID: NCT04357223 Recruiting - Overactive Bladder Clinical Trials

NOGO for an Overactive Bladder

NOGO-OAB
Start date: May 1, 2020
Phase: Phase 2
Study type: Interventional

This is a double-blind, randomized and placebo-controlled study to evaluate the safety and effectiveness of NoGo, a standardized extract from Angelica archangelica, on overactive bladder

NCT ID: NCT04305743 Recruiting - Clinical trials for Urinary Bladder, Overactive

Post-procedural Pain Associated With 5 Versus 20 Intravesical Injections of Onabotulinumtoxin A

Start date: October 9, 2019
Phase: Phase 4
Study type: Interventional

Currently, in clinical practice there has been no standardization in the number of injections a single dose of intradetrusor onabotulinumtoxin A is administered in. Given the increasing use of this treatment modality, the aim of this study is to compare outcomes for patients given a 100 unit dose of onabotulinumtoxin A split into 5 as compared to 20 injections for the treatment of overactive bladder or urgency urinary incontinence refractory to medical treatment.

NCT ID: NCT04075578 Recruiting - Bladder, Overactive Clinical Trials

Evaluation of Professional Practices in the Treatment of Refractory Idiopathic Overactive Bladder at the Dose of 50 Units (TOX50IUU)

TOX50IUU
Start date: June 26, 2019
Phase:
Study type: Observational

Considering that the 2013 Hermieu's guidelines differs from the product marketing authorization delivered in November 2014, the primary endpoints is to evaluate life quality by questionnaires at the baseline time, and after two, six and twelve weeks of treatment in patients suffer from urinary incontinence by refractory idiopathic overactive bladder and treated by Botox® at the dose of 50UI (international units)

NCT ID: NCT04059133 Recruiting - Overactive Bladder Clinical Trials

The Effect of Low Intensity Extracorporeal Low Energy Shock Wave Therapy on Stress Urinary Incontinence and Overactivity Bladder

Start date: February 27, 2018
Phase: N/A
Study type: Interventional

The hypothesis of the present study is low intensity extracorporeal low energy shock wave therapy (LiESWT) can decrease inflammatory disorders, increase pelvic floor blood supply, enhanced bladder stem cell activation, Using LiESWT can decrease bladder overactivity, eliminate urinary incontinence and improve stress urinary incontinence (SUI) and overactive bladder (OAB) symptoms. Therefore improve quality of life and improve social activity.

NCT ID: NCT04031014 Recruiting - Overactive Bladder Clinical Trials

High Intensity Focused Electromagnetic Field Device for Urinary Incontinence

Start date: February 1, 2020
Phase: N/A
Study type: Interventional

High intensity focused electromagnetic (HIFEM) technology induces deep pelvic floor muscle contractions designed to deliver the equivalent of 11,200 Kegel exercise over 28 minutes, with the intention of increasing neuromuscular tone of the pelvic floor. This study will have looking at treatment of the two of the most common pelvic floor disorders: stress or stress predominant urinary incontinence and urge or urge predominant urinary incontinence.