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Recruiting NCT07312461

Causes and Management of Children Presenting With Macroscopic Hematuria in the Pediatric Emergency Department

Observational Macroscopic Hematuria

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Macroscopic Hematuria. Basic parameters: up to 17 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Macroscopic hematuria. is a common symptom, leading to numerous emergency department visits in children of all ages. It can be linked to many pathologies, and its management in the emergency department is not standardized. Few articles describe the management of this symptom during pediatric emergency department visits. Therefore, it is important to study this symptom and its management in order to establish a protocol.

Primary outcome measures

  • Describe the different causes of this symptom [Time frame: Up to 12 months]

Eligibility criteria

Inclusion criteria

  • Minor subject (<18 years old)
  • Patient presenting to the pediatric emergency department with gross hematuria

Exclusion criteria

\- Subject (and/or their parents) who expressed their opposition to participating in the study.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Case-only

Study locations

France · 1 center
  • Service de Pédiatrie 1 - Réanimation - CHU de Strasbourg - France — Strasbourg

Identifiers

NCT: NCT07312461 · 9456

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗