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Not yet recruiting NCT07152951

Electrolytes Disturbance in Infant

Observational Electrolyte Disturbance in Gastrointestinal Diseases

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: Electrolyte Disturbance in Gastrointestinal Diseases. Basic parameters: 1 months — 4 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
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Prevalence of Electrolyte Disturbances in Infants and Children With Gastrointestinal Diseases

Overview

Prevalence of electrolyte disturbances in infants and children with gastrointestinal diseases

Detailed description

Prevalence of electrolyte disturbances in infants and children with gastrointestinal diseases

Primary outcome measures

  • 1-Determine prevalence and types of electrolyte disturbances in infants and children with gastrointestinal diseases [Time frame: From 1 Jan 2025 to 1 Jan 2026]

Eligibility criteria

Inclusion criteria

  • All patients from one month till 4 years who will be admitted to Gastroenterology unit in (AUCH) and diagnosed with a gastrointestinal disease

Exclusion criteria

  • 1-Neonates >1 month \& those <4 years . 2-Patients with acute or chronic kidney diseases that alter electrolyte balance. 3-Patients with endocrine disorders affecting electrolyte balance (e.g adrenal insufficiency). 4-Use of medications that alter electrolyte balance (e.g diuretics, steroids). 5-Critically ill patients that electrolyte disturbance is due to non-gastrointestinal causes.

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
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07152951 · AssuitUniversityAUH

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗