Condition 1: Nutritional support in intensive care. Condition 2: Nutritional support in intensive care. Unspecified severe protein-calorie malnutrition Other disorders of lung
Conditions
Interventions
Intervention 1: The enteral nutrition group will be the intervention group in a continuous manner. In the intervention group, enteral feeding will be done continuously (for 24 hours and in the form of
Sponsors
Kashan University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Being hospitalized in the intensive care unit Intestinal feeding through the nasogastric tube is prescribed by a doctor Have stable and normal hemodynamic conditions. The patient has a head trauma.
Exclusion criteria
Exclusion criteria: Age over 60 years The patient has intravenous nutrition The patient has a kidney or liver disorder
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Whole blood lymphocyte count. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood analyzer.;Blood hemoglobin level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood analyzer.;Hematocrit level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood analyzer.;Blood urea level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry test device.;Blood creatinine level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry device.;Blood calcium level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry device.;Blood phosphorus level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry device.;Blood phosphorus level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry device.;Blood cholesterol level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry device.;Blood triglyceride levels. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry device.;Blood aspartate aminotransferase level. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry device.;Remaining volume in the stomach. Timepoint: Daily. Method of measurement: Gavage syringe(50 cc).;Level of Albumin. Timepoint: Before intervention, 3 and 7 days after intervention. Method of measurement: Blood biochemistry test device.;Number of intestinal excretions. Timepoint: daily. Method of measurement: checklist.;Occurrence of pulmonary aspiration. Timepoint: daily. Method of measurement: checklist.;Number of vomiting. Timepoint: daily. Method of measurement: checklist.;Stomach | — |
Secondary
| Measure | Time frame |
|---|---|
| Weaning from the ventilator. Timepoint: End of intervention. Method of measurement: Checklist. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactIsmail Azizi-Fini
Kashan University of Medical Sciences
Outcome results
None listed