The Electroencephalographic Mechanisms of Anesthesia and Human Consciousness

Trial statusRecruiting
Trial phasePhase 4
Trial typeInterventional
Biological sexAll
Age3-65
SponsorGuangzhou General Hospital of Guangzhou Military Command

About this trial

In the field of general anesthesia research, the neural mechanism underlying the loss of consciousness has long been a highly core issue. It remains unclear what consciousness is and how it emerges from brain activity. By studying anesthesia and sleep, the investigators aim to reveal what happens in the brain when consciousness is lost and when it returns.

Dexmedetomidine, a widely used drug in clinical anesthetic practice, plays an important role in the anesthetic process due to its unique pharmacological properties. It hardly causes respiratory depression during the sedative and hypnotic process, which makes it occupy an important position in clinical anesthetic regimens.

The emergence of stereoelectroencephalography (SEEG) technology has brought new opportunities for research on anesthesia mechanisms. Compared with traditional electroencephalographic (EEG), SEEG can directly penetrate into deep brain structures to record electrical activities, enabling precise localization of brain regions closely related to consciousness regulation.

At present, although there have been some studies on the effects of dexmedetomidine on EEG activities, there are still many deficiencies. Most studies have focused on simple spectral analysis of EEG signals or observations of limited brain regions, lacking comprehensive multi-dimensional research on functional connectivity between brain regions, microstates, and complexity. Through monitoring key brain regions, the SEEG technology can obtain more targeted and accurate information, thereby providing strong support for comprehensively revealing the neural mechanisms of dexmedetomidine-induced loss of consciousness.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age range: 1 - 65 years old

BMI: 18.5 - 25.0 kg/m²

ASA physical status classification: I - III

Patients diagnosed with drug - refractory epilepsy who, after long - term monitoring of epileptic seizures, require stereo-electroencephalography (SEEG) electrode implantation based on the clinical need for monitoring their epilepsy.

Disqualifiers

Patients with severe arrhythmia or other organic heart diseases;

Patients with comorbid obstructive sleep apnea-hypopnea syndrome (OSAHS);

Patients with hepatic or renal dysfunction; those with a history of immunodeficiency diseases , or a history of cancer/malignant tumors, or a history of autoimmune diseases, or severe cardiovascular and cerebrovascular diseases, or other diseases that may significantly reduce life expectancy;

Patients with any history of diseases that may affect protocol compliance (such as severe mental disorders, disturbance of consciousness; cognitive dysfunction, drug abuse or addiction, etc.);

Trial design

Design model

Parallel

Treatments tested in this trial

  • Dexmedetomidine

    Drug

    Escalating concentrations until loss of responsiveness

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: SleepNo intervention 0 interventions
Group B: DexmedetomidineExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Stereo-electroencephalography

Time frame
After the patient has completed the monitoring of epileptic seizures due to clinical needs, they can participate in this test. Through test completion, an average of 3 hours.

Secondary outcomes

1

Functional connectivity

permutation mutual information (PMI); stereo-electroencephalography assessment parameter

Time frame
through test completion, an average of 3 hours
2

The complexity

examined by permutation entropy (PE); stereo-electroencephalography assessment parameter

Time frame
through test completion, an average of 3 hours
3

Phase-amplitude coupling (PAC)

PAC is used to illuminate cross-frequency coordination in neurophysiological activity of electroencephalogram. stereo-electroencephalography assessment parameter

Time frame
through test completion, an average of3 hours.
4

Directional connectivity

symbolic conditional mutual information (SCMI) and directionality index (DI); stereo-electroencephalography assessment parameter

Time frame
through test completion, an average of 3 hours

Other outcomes

Sponsors and contacts

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