CClinicalTrials.gg
RecruitingNCT06905600TPHAUpdated Apr 1, 2025

Transient Pseudohypoaldosteronism Affecting Children With Urinary Tract Malformation

An observational study in Pseudohypoaldosteronism, sponsored by University Hospital, Strasbourg, France. Recruiting at 1 site in France. Open to participants aged 1 Year to 6 Years. Per ClinicalTrials.gov, last updated 2025-04-01.

Sponsored by University Hospital, Strasbourg, France · Observational

From the registry’s dates

  • Primary completion was expected by Dec 2025, 10 months ago, but the record still lists the study as recruiting.
  • Started Jan 2024; still recruiting 2 years 8 months later.
Study type
Observational
Model
Case-control
Time perspective
Retrospective
Enrollment
50
Ages
1 Year to 6 Years
Sex
All
01

Study summary

Pseudohypoaldosteronism is a pathology affecting children under 6 months of age, little known but which can have serious consequences.

There are no real figures on the prevalence of this pathology in France. The exact pathophysiology is not known and the management is not currently codified.

This is why it is interesting to study this pathology and its treatment on a national scale in order to think about the best possible treatment, as well as to raise awareness of this pathology among different health professionals.

02

Conditions studied

  • Pseudohypoaldosteronism

Keywords

  • Pseudohypoaldosteronism
  • pseudohypoaldosteronism in children
03

In context

Lead sponsor

University Hospital, Strasbourg, France is the lead sponsor of 966 studies on the registry; 342 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
1 Year to 6 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Minor subjects aged less than 6 years at the time of diagnosis of pseudohypoaldosteronism in the context of urinary malformation and/or urinary infection between January 1, 2018 and December 31, 2023

Inclusion criteria

  • Minor subjects aged less than 6 years at the time of diagnosis
  • Diagnosis of pseudohypoaldosteronism in the context of urinary malformation and/or urinary infection between January 1, 2018 and December 31, 2023
  • Subject (and/or their parental authority) having not expressed, after information, their opposition to the reuse of their data for the purposes of this research.

Exclusion criteria

Exclusion Criteria:

  • Subject (or their parents) having expressed their (their) opposition to participating in the study
05

Study design

Observational model
Case-control
Time perspective
Retrospective
Enrollment
50 participants (estimated)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. National comparison of clinical and therapeutic practices concerning the management of pseudohypoaldosteronism in children with urinary malformations and/or urinary infections

    This study compares clinical and therapeutic practices The retrospective analysis of the data will be carried out using classic statistical tests (Student's test, Fisher's test, ROC curve)

    Time frame: Up to 1 year

07

Study locations

1 of 1 sites recruiting
  • Service pédiatrie 1 - CHU de Strasbourg - France
    Strasbourg, 67091, France
    • Ariane ZALOSZYC, MD · Contact · ariane.zaloszyc@chru-strasbourg.fr · 33 3 88 12 77 42
    • Ariane ZALOSZYC, MD · Principal investigator
    • Inès BERNHARD, MD · Sub investigator
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 1, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06905600
Lead sponsor
University Hospital, Strasbourg, France
Responsible party
Sponsor
First posted
Apr 1, 2025
Start date
Jan 31, 2024
Primary completion
Dec 2025 (estimated)
Completion
Dec 31, 2025 (estimated)
Last update
Apr 1, 2025

Study contacts

Ariane ZALOSZYC, MD
Contact
ariane.zaloszyc@chru-strasbourg.fr
33 3 88 12 77 42

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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