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Overactive Bladder clinical trials

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NCT ID: NCT03087578 Withdrawn - Overactive Bladder Clinical Trials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: NCT03080389 Terminated - Overactive Bladder Clinical Trials

Sensitivity of Extended Cultures in Diagnosing Urinary Tract Infections

Start date: July 1, 2017
Phase:
Study type: Observational

There is some evidence to suggest standard urine cultures may not be adequate in identifying patients with low grade urinary tract infections. Therefore, there are patients with symptoms of frequency and urgency, being misdiagnosed with overactive bladder due to negative urine cultures. If this is true, could extended cultures be used to identify the false negative patients?

NCT ID: NCT03061760 Not yet recruiting - Prostate Cancer Clinical Trials

Effects of Urinary Bladder Hypertrophy on Urge Urine Incontinence After Radical Prostatectomy

Start date: March 1, 2017
Phase: N/A
Study type: Observational

This study is designed to evaluate men before radical prostatectomy for the incidence of Overactive Bladder (OAB), as well as urge urine incontinence (UUI) development after the surgery. Patients will be evaluated for signs of OAB and for signs of Bladder Outlet Obstruction (BOO). Afterwards they will be divided into four observational groups. Follow up period is designed to be 12 months.

NCT ID: NCT03057158 Completed - Insulin Resistance Clinical Trials

Genomics and Epigenomics for New Insights in fEmale OAB (GENIE) Study

GENIE
Start date: May 1, 2017
Phase:
Study type: Observational

Millions of women suffer from overactive bladder, and the changes in bladder function affect their quality of life. The study team believes that it needs to be better understand why women get overactive bladder in the first place so that better treatments can eventually be offered. The purpose of this study is to determine why women with insulin resistance are more likely to get overactive bladder. Overactive bladder is a type of bladder control problem that can cause some women to have bladder leakage. This problem is more common in women with diabetes and pre-diabetes, but it isn't known why.

NCT ID: NCT03023241 Completed - Overactive Bladder Clinical Trials

Diagnosis of Bladder Pain Syndrome / Interstitial Cystitis

Start date: December 2004
Phase: N/A
Study type: Interventional

To identify new, simple and reliable biomarkers for bladder pain syndrome/interstitial cystitis (BPS/IC) for diagnosis of this disease.

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: NCT03017170 Completed - Overactive Bladder Clinical Trials

Evaluation of the Effect of Dried Cranberry Powder in Women With Dry OAB

Start date: April 2016
Phase: Phase 1
Study type: Interventional

A randomized, double-blind, placebo controlled study to evaluate the efficacy of dried cranberry at 500 mg daily in women with overactive bladder for 6-months.

NCT ID: NCT02995967 Terminated - Overactive Bladder Clinical Trials

Evaluation of Botulinum Toxin A Alone Versus Botulinum Toxin A With Hydrodistension for Treatment of Overactive Bladder

HydrA
Start date: November 2016
Phase: N/A
Study type: Interventional

The specific aim of this trial is to determine if hydrodistention at the time of intradetrusor injection of botulinum toxin A has additional benefit in patients with refractory overactive bladder (OAB) and urgency symptoms compared to intradetrusor injection of botulinum toxin A alone. Consented patients will be randomized to hydrodistention at a pressure of 80 cm H2O for 5 minutes, prior to the intradetrusor injection of 100 units of botulinum toxin A (hydrodistention group) or intradetrusor injection of 100 units of botulinum toxin A alone (botulinum toxin A alone group). The primary aim will be subjective improvement measured as change from baseline at 12 weeks using the OAB-q bother subscale.

NCT ID: NCT02980328 Not yet recruiting - Clinical trials for Urinary Incontinence

Low-level Light Therapy for Overactive Bladder and Urinary Incontinence

Start date: December 2016
Phase: Phase 3
Study type: Interventional

This study aims to evaluate the effectiveness of a self-therapeutic approach of skin adhesive low-level light therapy (LLLT) in females with Overactive Bladder (OAB) and Urinary Incontinence (UI)

NCT ID: NCT02940314 Completed - Overactive Bladder Clinical Trials

Safety and Pharmacokinetic Characteristics After Administration of HIP1503 and HGP1103 in Healthy Male Volunteers

Start date: March 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to compare the safety and pharmacokinetic characteristics after administration of HIP1503 and HGP1103 in healthy male volunteers.