Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04413461
Other study ID # 19-HPNCL-03
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date January 13, 2021
Est. completion date May 2025

Study information

Verified date September 2023
Source Fondation Lenval
Contact Ronny Bensaid, MD
Phone 0492030303
Email bensaid.r@pediatrie-chulenval-nice.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Nocturnal enuresis is a functional urinary disorder in children. It is intermittent urinary incontinence during sleep in children aged 5 years and older. It is said to be "primary" if the child has never been clean at night for at least 6 months and "isolated" if there are no other associated urinary symptoms, including daytime symptoms. It is a common condition with significant repercussions, including disruption of family and social life and a frequent decline in self-esteem. Without treatment, it can persist into adulthood. All these reasons justify taking care of these children. This is usually based on: The establishment of hygienic-dietetic rules: Regular urination and before sleeping, limitation of fluid intake in the evening. They are systematically implemented, whatever the subsequent management Drug treatments (Desmopressin, oxybutynin). These treatments have an efficiency of 60 to 70% at 6 months post treatment and sometimes have side effects. Non-drug treatments: Night-time "pee stop" alarms. They have an efficiency of around 70%. They are little used because they often wake up the whole family and are not reimbursed by social security. TENS (Transcutaneous Electro Neuro Stimulation) is a neuro-modulation technique which consists of stimulating the nerves by means of skin electrodes in order to obtain a somatic response. In urology, it is mainly used by stimulating either the sacral region, origin of the vesical innervation, or the tibial nerve. Its main indication is overactive bladder, a source of discomfort and incontinence. It is used at home, the side effects are exceptional and it does not disturb the activities of the patients. Few studies have evaluated its effectiveness in isolated primary enuresis.


Description:

Nocturnal enuresis is a functional urinary disorder in children. It is intermittent urinary incontinence during sleep in children aged 5 years and older. It is said to be "primary" if the child has never been clean at night for at least 6 months and "isolated" if there are no other associated urinary symptoms, including daytime symptoms. It is a common condition with significant repercussions, including disruption of family and social life and a frequent decline in self-esteem. Without treatment, it can persist into adulthood. All these reasons justify taking care of these children. This is usually based on: The establishment of hygienic-dietetic rules: Regular urination and before sleeping, limitation of fluid intake in the evening. They are systematically implemented, whatever the subsequent management Drug treatments (Desmopressin, oxybutynin). These treatments have an efficiency of 60 to 70% at 6 months post treatment and sometimes have side effects. Non-drug treatments: Night-time "pee stop" alarms. They have an efficiency of around 70%. They are little used because they often wake up the whole family and are not reimbursed by social security. TENS (Transcutaneous Electro Neuro Stimulation) is a neuro-modulation technique which consists of stimulating the nerves by means of skin electrodes in order to obtain a somatic response. In urology, it is mainly used by stimulating either the sacral region, origin of the vesical innervation, or the tibial nerve. Its main indication is overactive bladder, a source of discomfort and incontinence. It is used at home, the side effects are exceptional and it does not disturb the activities of the patients. Main objective is to compare the effectiveness of treatment with TENS versus TENS sham procedure (placebo) in isolated primary enuresis, one month after the end of treatment in patients from 5 to 17 years old The effectiveness will be evaluated by the evolution of the number of wet nights


Recruitment information / eligibility

Status Recruiting
Enrollment 74
Est. completion date May 2025
Est. primary completion date January 2025
Accepts healthy volunteers No
Gender All
Age group 5 Years to 17 Years
Eligibility Inclusion Criteria: Children 5 to 17 years old - Medium or severe isolated primary enuresis (more than 1 episode per week) - Never treated or in failure of previous treatment (with treatment discontinuation for at least 1 month) - Affiliation to a social security scheme - Good understanding of the protocol - Signature of informed consent by a parent or the legal representative of parental authority Exclusion Criteria: Other pathologies which can influence urination behavior (Daytime urinary disorders) - Treatment in progress which can modify voiding behavior - TENS treatment in progress for another pathology

Study Design


Intervention

Other:
TENS
Transcutaneous Electro Neuro Stimulation
TENS Sham
placebo of Transcutaneous Electro Neuro Stimulation : similar device without electro stimulation

Locations

Country Name City State
France CH de Cannes Cannes
France CH de GRASSE Grasse
France CHU de Nice Nice
France Hôpitaux Pédiatrique de Nice CHU Lenval Nice

Sponsors (1)

Lead Sponsor Collaborator
Fondation Lenval

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary effectiveness of treatment with Transcutaneous Electro Neuro Stimulation (TENS) versus TENS sham procedure at 1 month post treatment The effectiveness will be evaluated by the evolution of the number of wet nights.
Measure of number of wet nights per week at baseline before treatment by TENS and at 1 month after the end of treatment
at 2 months
Secondary effectiveness of treatment with TENS versus TENS sham procedure at 1 month measure of number of wet nights per week at the end of treatment at 1 month
Secondary quality of life during treatment measure of quality of life with the Pediatric Quality of Life Inventory (Peds QL) questionnaire.
The Pediatric Quality of Life Inventory (PedsQL) is a 23-items generic health status instrument with parent and child forms that assesses five domains of health (physical functioning, emotional functioning, psychosocial functioning, social functioning, and school functioning) in children and adolescents ages 2 to 18.
For ease of interpretability, items are reversed scored and linearly transformed to a 0-100 scale, so that higher scores indicate better HRQOL (Health-Related Quality of Life). The minimum value is 0 and maximum is 100.
at baseline and at 1 month and at 2 month
See also
  Status Clinical Trial Phase
Completed NCT03389412 - The Effect of Selecting Treatment With Desmopressin or Alarm to Children With Enuresis Based on Home Recordings. Phase 4
Completed NCT04260646 - Alarm Treatment for Combined Enuresis and Daytime Urinary Incontinence in Children N/A
Recruiting NCT03522818 - Enuresis Alarm - Is a Manual Trigger System Beneficial? N/A
Recruiting NCT05126732 - Ganglion Cell Thickness in Enuresis Nocturna
Completed NCT03543995 - The Relationship Between Nocturnal Enuresis And Spina Bifida Occulta
Completed NCT05151081 - Overactive Bladder Syndrome
Active, not recruiting NCT06185361 - Selective Serotonin Reuptake Inhibitors, Fluoxetine Versus the Standard Oral Desmopressin for Management of Mono-symptomatic Nocturnal Enuresis. N/A
Completed NCT04280887 - MyPad - Intelligent Bladder Pre-void Alerting System N/A