About this trial
The goal of this observational retrospective study is to evaluate the electroencephalography (EEG)'s poficiency in the treatment of neuroelectric stimulation in patients with severe traumatic brain injuries (TBI).
The main questions it aims to answer are:
1. Whether EEG of patients with severe TBI will change after they receiving neuroelectrial stimulation? If yes, how does it change? 2. How can EEG be used to evaluate the condition of patients with severe TBI?
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
7 days after severe traumatic brain injuries (GCS score 3-8);
Over 18 years old, regardless of gender;
The patient's legal representative is informed and voluntarily signs the consent form.
Disqualifiers
Unstable vital signs;
History of mental disorders or neurodegenerative diseases;
Uncontrolled epilepsy;
Severe arrhythmias or patients with implanted cardiac pacemakers;
Trial population
Patients have severe TBI and receive neuroelectral stimulation.
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
CRS-R scores 6 months after the patient's discharge
Using the COMA RECOVERY SCALE-REVISED (CRS-R) to evaluate the condition of the patient 6 months after discharge and the effectiveness of neuroelectrial stimulation. The minimum and maximum values of CRS-R is 0 and 23 and higher scores mean a better outcome.
Secondary outcomes
CRS-R scores during hospitalization
Using the COMA RECOVERY SCALE-REVISED (CRS-R) to evaluate the condition of the patient during hospitalization and the effectiveness of neuroelectrial stimulation. The minimum and maximum values of CRS-R is 0 and 23 and higher scores mean a better outcome.
Sponsors and contacts
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