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Urinary Bladder, Underactive clinical trials

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NCT ID: NCT06452927 Not yet recruiting - Clinical trials for Lower Urinary Tract Symptoms

EEP in Patients With Urodynamically Proven DU/DA

Start date: September 2024
Phase: N/A
Study type: Interventional

The aim of this project is to create und evaluate a multicentral, retro-/prospective database for patients with urodynamically proven detrusor underactivity (DU) or acontractility (DA) secondary to a non-neurogenic aetiology, who undergo endoscopic, anatomic enucleation of the prostate (EEP).

NCT ID: NCT06020963 Recruiting - Clinical trials for Detrusor Underactivity

Can Acupoint Low Intensity Shockwave Therapy Improve Bladder Voiding Efficiency

Start date: August 11, 2023
Phase: N/A
Study type: Interventional

With the increasing of the elderly population, patients with urinary dysfunction caused by inefficiency of bladder emptying becomes much often than before. However, the current treatments for this kind of bladder dysfunction are limited and unsatisfactory. Low-intensity extracorporeal shockwave therapy (LiESWT) is a very popular emerging treatment in recent years, and abundant of literatures have confirmed that this treatment is safe and effective in myofascial pain and male erectile dysfunction. Recently, many animal experiments have showed that LiESWT could improve urinary dysfunction caused by bladder dysfunction. Taiwan based studies also reported that LiESWT could improve symptoms of overactive bladder. LiESWT is a non-drug, low-invasive and high-safety treatment, which is very suitable for elderly patients. In this study investigator combine the LiESWT and acupuncture to treat the patients with underactive bladder. Investigator hypothesize that LiESWT could improve bladder voiding efficiency.

NCT ID: NCT05576311 Not yet recruiting - Clinical trials for Urinary Incontinence

Codesign of an Optical Device to Measure Urine Flow and Volume

Start date: November 1, 2022
Phase:
Study type: Observational

The study is seeking to understand the needs of patients and healthcare practitioners for an innovation in the way that changes in bladder function are assessed. This information will be used in the design and evaluation of a device, being developed in parallel, that assesses changes to the volume and flow of urine in order to determine changes in bladder function. In order to ensure development is optimal, the principal research objective is therefore to understand the needs of patients and healthcare practitioners (ranging from care home staff and GPs in primary care, to urologists in tertiary referral centres).

NCT ID: NCT05485142 Recruiting - Overactive Bladder Clinical Trials

The Treatment Efficacy of Prolotherapy in Bladder Voiding Dysfunction

Start date: May 1, 2019
Phase: N/A
Study type: Interventional

Voiding dysfunction including overactive bladder, underactive bladder, and neuropathic bladder. Voiding dysfunction has a great impact on life quality, especially in the elderly society. The current medication for overactive bladder has limited efficacy and the patient easily to dropout the medication because of its side-effects. The underactive bladder is a new entity of voiding dysfunction, its optimal is still unknown. Sacral neuromodulation(SNM) and posterior tibial nerve stimulation(PTNS) have been applied for both overactive bladder and underactive bladder treatment and the results is promising, but the equipment of SNM or PTNS is not available in most places. Prolotherapy using glucose local injection causing inflammatory reaction to stimulate cytokine and growth factors release. Investigators combined the concepts of posterior tibial nerve stimulation and prolotherapy to treat voiding dysfunction. Investigators anticipate it maybe a new promising treatment for voiding dysfunction.

NCT ID: NCT05470751 Completed - Multiple Sclerosis Clinical Trials

GentleCathâ„¢ for Men Intermittent Catheter With FeelCleanâ„¢ Technology

Start date: February 2, 2023
Phase:
Study type: Observational

Male self catherterisng observational study.

NCT ID: NCT05359484 Completed - Clinical trials for Detrusor Underactivity

Delta Q Value to Discriminate Detrusor Underactivity From Bladder Outlet Obstruction

Start date: January 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

To determine the significance of delta Q value (Qmax - Qave) in discrimination between BOO and DU, to avoid invasive studies (pressure flow studies (PFSs)) and replace them with noninvasive study (uroflowmetry).

NCT ID: NCT04981080 Completed - Clinical trials for Bladder Outlet Obstruction

DU and BOO in Women With and Without Symptoms of VD

Start date: February 1, 2005
Phase:
Study type: Observational

Women with symptoms of voiding dysfunction may be associated with detrusor underactivity or bladder outlet obstruction. However, the prevalence of detrusor underactivity and bladder outlet obstruction remained obscure. Thus, the aim of this study was to elucidate the prevalence of detrusor underactivity and bladder outlet obstruction in women with and without symptoms of voiding dysfunction.

NCT ID: NCT04543552 Completed - Neurogenic Bladder Clinical Trials

A Comparative Analysis of Portable Bladder Scanner to Determine Age/ Volume Specific Accuracy in 0-6 Years of Children

Start date: November 13, 2017
Phase:
Study type: Observational

As a part of the urodynamic studies, urinary catheterization is inserted to measure residual urine, however, it has shown to be an invasive procedure, cause urinary tract infection, and traumatic experience. Bladder scan has been introduced as an alternative and non-invasive method to measure urine residual in the bladder.

NCT ID: NCT04516434 Recruiting - Clinical trials for Urinary Bladder, Underactive

Amplifying Sensation in Underactive Bladder

AMPLIFY
Start date: September 1, 2021
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the influence of intravesical (bladder) electrical stimulation and intraurethral electrical stimulation on bothersome symptoms and bladder function in neurologically-intact adult women with underactive bladder. The investigators hypothesize that electrical stimulation will decrease bothersome urinary symptoms relative to baseline and increase voided percentage during pressure-flow studies compared to their routine clinical exam.

NCT ID: NCT04473469 Completed - Urinary Retention Clinical Trials

Previously Implanted Pudendal Nerve Stimulation

Start date: January 19, 2021
Phase: N/A
Study type: Interventional

This study seeks to examine the response of the bladder to different pudendal nerve stimulation frequencies, by studying patients who have been previously-implanted with pudendal nerve neurostimulators.