Effect of intravenous fluid sodium concentration on plasma sodium in pediatric patients
- Conditions
- Hyponatremia.Hypo-osmolality and Hyponatremia
- Registration Number
- IRCT2013121015740N1
- Lead Sponsor
- Vice chancellor for research, Tehran Univercity of Medcal Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
children in the age range 30 days to 14 years for his doctor prescribe intravenous fluid and pain for at least 24 hours in hospital pediatric intensive care Bahrami,Tehran University of Medical are admitted users.
Exclusion criteria: patients with acute or chronic renal parenchymal problems, such as diabetic ketoacidosis and cerebral edema in patients at risk of trauma to the head, heart disease; hypoglycemic patients; patients with abnormal secretion of antidiuretic hormone; diabetes insipidus; pituitary or hypothalamic disorders. patients underwent surgery to have lost a lot of blood during surgery, and cranial thoracic surgery patients; cirrhotic patients; patients with severe malnutrition; diabetes, and his doctor to his patient fluid therapy in a framework designed this study can not reject.
Withdrawal criteria; The research indicates that children with higher serum sodium lower than the normal range (135_145); the need to take CPR; being intubated; the death; early oral feeding; or any condition that a doctor's decision to withdraw his case if the study or decide to change intravenous fluids may be excluded.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Plasma concentrations of sodium. Timepoint: 24 hours after initiation of intravenous fluid. Method of measurement: Sodium concentration in the blood sample.
- Secondary Outcome Measures
Name Time Method Complications Haypvnatrmy. Timepoint: During and after reading. Method of measurement: Clinical interviews with hospital doctors.