Electroencephalography in the Management of Neuroelectric Stimulation in Patients With Severe Traumatic Brain Injuries

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorRenJi Hospital

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 volunteers

Qualifiers

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

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

50 Participants
are grouped into 2 trial groups
Group A: Consicousness improved group
Group B: Consicousness unimproved group

Trial outcomes

Primary outcomes

1

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.

Time frame
6 months

Secondary outcomes

1

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.

Time frame
3 months

Other outcomes

Sponsors and contacts

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