Electroencephalography in the Management of Neuroelectric Stimulation in Patients With Severe Traumatic Brain Injuries
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: Brain Injuries. Basic parameters: from 18 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
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of Electroencephalography in the Management of Neuroelectric Stimulation in Patients With Severe Traumatic Brain Injuries: A Prospective Study
Overview
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?
Primary outcome measures
- CRS-R scores 6 months after the patient's discharge [Time frame: 6 months]
Secondary outcome measures (1)
- CRS-R scores during hospitalization [Time frame: 3 months]
Eligibility criteria
Inclusion criteria
- 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.
Exclusion criteria
- Unstable vital signs;
- History of mental disorders or neurodegenerative diseases;
- Uncontrolled epilepsy;
- Severe arrhythmias or patients with implanted cardiac pacemakers;
- Various conditions that interfere with scalp EEG collection;
- Pregnant women.
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
- Cohort
Study locations
China · 1 center
- Brain Injury Center, Renji Hospital, School of Medicine, Shanghai Jiao Tong University — Shanghai
Identifiers
NCT: NCT06571032 · LY2024-007