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Nocturnal Enuresis clinical trials

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NCT ID: NCT06243042 Completed - Nocturnal Enuresis Clinical Trials

Vitamin D Serum Levels in Monosymptomatic Enuretic and Non Enuretic Children

Start date: February 12, 2020
Phase:
Study type: Observational

We are group of researchers interested in causes and management of nocturnal enuresis, we embarked on this research on 2020 and we reached promising results regarding the role of vitamin D serum level in etiology and management of monosymptomatic enuresis.

NCT ID: NCT05368246 Completed - Clinical trials for Urinary Incontinence

Safety and Performance of UCon for the Treatment of the Symptoms of Overactive Bladder (OAB) / Bowel Dysfunction (BD)

Start date: February 15, 2022
Phase: N/A
Study type: Interventional

This clinical investigation is a single-arm, prospective, multicentre, early feasibility study, which is used to evaluate the device design of UCon with respect to initial clinical safety and device performance in a small number of subjects. UCon is a medical device for treatment of the symptoms of overactive bladder (OAB) and bowel disorders (BD). It electrically stimulates the dorsal genital nerve (DGN) through the skin to obtain modulated behaviour of the bladder/bowel musculature e.g., suppress undesired bladder/bowel activity to relieve the symptoms of the patient.

NCT ID: NCT05190601 Completed - Enuresis Clinical Trials

Uroflowmetry in Children With Enuresis Nocturnal

Start date: January 1, 2020
Phase:
Study type: Observational [Patient Registry]

Background: Enuresis nocturna is an important social and psychological problem in children. Uroflowmetry is an important test used to investigate lower urinary tract symptoms.. Objective:To evaluate the uroflowmetry (UFM) results of children with nocturnal enuresis (NE). Method: The uroflowmetry findings of healthy and visualized children without any urinary symptoms and who were prospectively admitted to the urology and pediatric surgery outpatient clinic with the complaint of Enuresis nocturna between January 2020 and July 2021 were compared. Information (anamnesis, physical examination, radiology results and laboratory tests) and uroflowmetry results of NE and healthy children included in the study were recorded.

NCT ID: NCT05178641 Completed - Nocturnal Enuresis Clinical Trials

Overnight Pant Study for Children With Nocturnal Enuresis

Start date: January 13, 2022
Phase: N/A
Study type: Interventional

This study will evaluate the in-use tolerance of an absorbent disposable underwear pant developed for children with nocturnal enuresis by assessing adverse events. In addition product performance will be assessed by the parent at home via a daily diary.

NCT ID: NCT05151081 Completed - Clinical trials for Overactive Bladder Syndrome

Overactive Bladder Syndrome

Start date: February 3, 2020
Phase:
Study type: Observational

Purpose: A lot of etiological factors related to overactive bladder (OAB) has been investigated. However, the role of primary nocturnal enuresis (NE), which is characterized with childhood night time incontinence, in the etiology of OAB is controversial. This study aims to evaluate the effect of NE in patients diagnosed with OAB. Metod Between january-september 2021, the data of patients who applied to the urology outpatientclinic with OAB symptoms were collected. Patients with a history of chronic systemic disease, previous medical treatment for OAB and who did not accept to join the study were excluded. According to the diagnosis of childhood NE, patients were divided into two groups. Demographic data hav been recorded. Frequency of incontinence, number of day time void and nocturia were evaluated according to a 3 day voiding diary. Inaddition, max. Urinary flowr atio (Qmax), bladder Wall thickness and postvoid residual volüme rates were determined using uroflowmetry and pelvic ultrasound.

NCT ID: NCT04280887 Completed - Enuresis Clinical Trials

MyPad - Intelligent Bladder Pre-void Alerting System

MyPad
Start date: August 3, 2018
Phase: N/A
Study type: Interventional

Development a 'dry alarm' that can help children and adolescents become dry at night.

NCT ID: NCT04260646 Completed - Clinical trials for Incontinence, Urinary

Alarm Treatment for Combined Enuresis and Daytime Urinary Incontinence in Children

ABDE
Start date: May 1, 2017
Phase: N/A
Study type: Interventional

The aim is to examine whether alarm therapy in addition to urotherapy can have a beneficial effect in treating urinary incontinence children with combined daytime incontinence and enuresis. The study will include children who suffers for combined daytime incontinence and enuresis and referred to one of the pediatric departments were offed to participate. Participants are randomized to 8 weeks treatment with either enuresis alarm and timer watch assist urotherapy or solely timer watch assisted urotherapy.

NCT ID: NCT04191863 Completed - Epilepsy Clinical Trials

Sleep Architecture in Valproate-induced Nocturnal Enuresis in Primary School and Preschool Children.

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

Our study, retrospectively evaluate the characteristics of and the risk factors for the occurrence of nocturnal enuresis in epileptic children kept on valproate monotherapy. Epileptic children with the age ranged 5 up to 15 years who were started and kept up on valproate monotherapy. In this study, a child determined to have nocturnal enuresis based on the American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders, fourth edition: "an involuntary voiding of urine during sleep, with a severity of at least twice a week, in children aged 5 years or older, in the absence of congenital or acquired defects of the nervous system."

NCT ID: NCT04049019 Completed - Nocturnal Enuresis Clinical Trials

Biomarkers in Urine for Children With Monosymptomatic Nocturnal Enuresis and Nocturnal Polyuria

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

The aim of the study is to identify protein markers in relation to the enuresis related nocturnal polyuria by using mass spectrometry on nocturnal urine samples. A biomarker for nocturnal polyuria would simplify an important part of the clinical characterization of enuresis patients.

NCT ID: NCT03883724 Completed - Nocturia Clinical Trials

Impact of Behavioral Treatment of Insomnia on Nighttime Urine Production

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

Nocturia is prevalent in older adults and it vastly reduces quality of life. Yet its treatment remains inadequate because its causes are not well understood, especially nocturnal polyuria or increased urine production at night. This study, which builds on the investigators' ongoing research, would be the first of its kind to explore the role of sleep in nighttime urine production. The findings will contribute important knowledge to guide development of better targeted and more effective therapy for this prevalent and morbid condition.