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NCT06439862Recruiting

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

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

Source: ClinicalTrials.gov · Last updated 5 Aug 2026

Brief summary (registry, in English)

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).

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
28 May 2024
Start date
20 Aug 2024
Primary completion date
Aug 2028
Lead sponsor
Hospices Civils de Lyon
NCT number
NCT06439862

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 20 Aug 2024 to the primary completion date, Aug 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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

Who the study is looking for

  • 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

Age in the registry: 6 years to 17 years · Sex: Male

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Femme-Mère-Enfant Hospital
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BronFranceRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.