Traumatic brain lesions. Intracranial injury
Conditions
Interventions
Intervention 1: Patients in the beta-blocker treatment group received 0.5 mg per kg of propranolol orally every 12 hours from the start of hospitalization until the day of discharge. Intervention 2: C
Sponsors
Shiraz University of Medical Sciences
Eligibility
Sex/Gender
All
Age
No minimum to 15 Years
Inclusion criteria
Inclusion criteria: Children with Traumatic Brain Injuries Parental consent to participate in the study Injury Severity Scale less than 3 in chest and abdomen
Exclusion criteria
Exclusion criteria: Age over 15 years Injury Severity Scale greater than 3 in chest and abdomen Parental non-consent to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Mortality rate. Timepoint: From the beginning to the end of the study. Method of measurement: The number of dead people divided by the total number of patients in each group.;GOSE is a measure for assessing patients' functional outcomes and their level of dependency following an injury. Timepoint: At the time of discharge, 3 and 6 months after discharge. Method of measurement: It was measured using the Glasgow Coma Scale and scoring it. Scoring: from 1 (death) to 5 (significant improvement), where higher scores indicate better outcomes and greater independence.;Length of stay in PICU. Timepoint: From the beginning to the end of the study. Method of measurement: The number of days between the admission date and the discharge date of the patient from PICU.;Length of hospital stay. Timepoint: From the beginning to the end of the study. Method of measurement: The number of days between the admission date and the discharge date of the patient from hospital. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactMohammad Sadegh Masoudi
Shiraz University of Medical Sciences
Outcome results
None listed