Study of the Quality of Life in School Aged-children With Posterior Urethral Valves

NCT ID: NCT06439862

Last Updated: 2025-05-07

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

300 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-08-20

Study Completion Date

2026-08-31

Brief Summary

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Posterior urethral valves (PUV) are the most common congenital obstructive lesion of the urethra, affecting from 1 per 3000 to 1 per 8000 live births. Valve ablation usually resolves the obstruction in PUV but patients still may suffer of deterioration in renal and urinary functions.

Renal insufficiency is the most feared long-term complication. Up to 50 % of the patients will develop chronic kidney disease (CKD), and up to 20 % will develop end-stage renal disease (ESRD) and ultimately will require kidney transplantation. PUV is the first urological cause of ESRD. Progression towards CKD depends on febrile urinary tract infections (UTIs), severity of a vesicoureteral reflux and bladder dysfunction.

Bladder dysfunction is due to an overactive and small poorly compliant bladder during infancy. Detrusor overactivity usually decreases in childhood and bladder capacity increases. The most common symptom of this bladder dysfunction is urinary incontinence. 60 % of children are continent at the age of 5 years old and 90 % at 10 years old. In case of persistent bladder dysfunction, medical treatment (anticholinergics, alpha-blockers) may be introduced, or even intermittent catheterizations.

Current scientific literature has very few studies on quality of life (QoL) in patients with PUV, mostly in adult patients and very small cohorts. Men treated for PUV in childhood had a good quality of life compared to the normative population, except for sleeping, eating and sexual activity. It seemed that the more severe the urological and nephrological functions were, the lower the QoL was. Children were only asked about intermittent urinary catheterization, and family point of view has never been collected. However, QoL and long-term evolution represent the first concerns of parents-to-be in prenatal counseling, or after diagnosis in an infant with PUV.

Hence, the aim of the study is to investigate the quality of life in school-aged children who had been treated for PUV in their first year of life, as measured by the Pediatric Quality of Life Inventory Version 4.0 (PedsQL 4.0).

Detailed Description

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Conditions

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Quality of Life Posterior Urethral Valve Renal Insufficiency Chronic Renal Disease End Stage Renal Disease Bladder Dysfunction Urinary Incontinence

Study Design

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Observational Model Type

CASE_ONLY

Study Time Perspective

RETROSPECTIVE

Interventions

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Children with PUV

Male children aged 6 to 17 years old treated for PUV in their first year of life between 2006 and 2018 in Lyon, and managed in the Femme-Mère-Enfant Hospital in Lyon

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Male patients and their parents/relatives
* Aged 6 to 17 years old
* Treated for PUV in their first year of life between 2006 and 2018
* Managed in the Femme-Mère-Enfant Hospital in Lyon

Exclusion Criteria

* Children with pre-existing severe cognitive and physical disability (physician's rating) from other condition
* Children enable to complete QoL questionnaire due to mental or communication impairment
Minimum Eligible Age

6 Years

Maximum Eligible Age

17 Years

Eligible Sex

MALE

Accepts Healthy Volunteers

No

Sponsors

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Hospices Civils de Lyon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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BIDAULT Valeska, MD

Role: PRINCIPAL_INVESTIGATOR

Hospices Civils de Lyon

Locations

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Femme-Mère-Enfant Hospital

Bron, Bron, France

Site Status RECRUITING

Countries

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France

Central Contacts

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BIDAULT Valeska, MD

Role: CONTACT

04 27 85 57 94

Facility Contacts

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BIDAULT Valeska, MD

Role: primary

04 27 85 57 94

LO Claire, MD

Role: backup

Other Identifiers

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69HCL24_0181

Identifier Type: -

Identifier Source: org_study_id

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