Not yet recruiting NCT07152951
Electrolytes Disturbance in Infant
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 →
Unsure about the terms? Read our patient guide →
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