Prevelance of Hypercalciuria in Children With Steroid Dependent Nephrotic Syndrome
1 other identifier
observational
50
1 country
2
Brief Summary
Prevelance of hypercalciurea in children with sterorid dependent nephrotic syndrome
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2024
Typical duration for all trials
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 1, 2024
CompletedFirst Submitted
Initial submission to the registry
September 19, 2025
CompletedFirst Posted
Study publicly available on registry
September 26, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2026
CompletedSeptember 26, 2025
September 1, 2025
2 years
September 19, 2025
September 19, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Prevalence of hypercalciurea
At enrollment
Study Arms (1)
Children with steroid dependent nephrotic syndrome
Participants will undergo urine analysis to measure calcium excretion in order to assess the prevalence of hypercalciuria. No experimental treatment will be given.
Eligibility Criteria
Children diagnosed with steroid-dependent nephrotic syndrome who are being followed up at the pediatric nephrology clinic.
You may qualify if:
- \- Age between 2 and 16 years.
- Diagnosis of steroid-dependent nephrotic syndrome (according to standard clinical criteria).
- Currently in remission or relapse while on steroid therapy.
You may not qualify if:
- \- Children with congenital or secondary nephrotic syndrome.
- Presence of other chronic kidney diseases.
- Use of medications that affect calcium metabolism (other than steroids).
- Children with systemic diseases affecting bone or mineral metabolism.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (2)
Sohag university hospital
Sohag, 82524, Egypt
Sohag university hospital
Sohag, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- CROSS SECTIONAL
- Target Duration
- 1 Day
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Ahmed ewees
Study Record Dates
First Submitted
September 19, 2025
First Posted
September 26, 2025
Study Start
January 1, 2024
Primary Completion
January 1, 2026
Study Completion
April 1, 2026
Last Updated
September 26, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share
De-identified individual participant data (IPD) that underlie the results of the study will be made available upon reasonable request from the principal investigator, after publication of the main results.