Skip to content

High-density TMS-EEG and multi-omics dynamic mapping of neurobiological trajectories of recovery of consciousness after general anesthesia

High-density TMS-EEG and multi-omics dynamic mapping of neurobiological trajectories of recovery of consciousness after general anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600127980
Enrollment
Unknown
Registered
2026-07-11
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delayed awakening and disturbance of consciousness after general anesthesia

Interventions

Patients receiving Propofol intravenous anesthesia:None

Sponsors

Xuzhou Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged 18-65 years; 2.ASA I class; 3.Elective, laparoscopic surgery estimated to last 2-4 hours; 4.Able to understand and voluntarily sign written informed consent.

Exclusion criteria

Exclusion criteria: 1.History of any diagnosed mental disorder that may affect cognition or mood; 2.History of neurological disease; 3.Skull or scalp injuries or defects, or skin diseases or anatomical abnormalities that may affect stable wearing of the EEG cap and accurate positioning of the TMS; 4.Having metal implants in the body; 5.Long-term use of any drug that may affect the central nervous system; abuse of alcohol or psychoactive substances; 6.Have a history of allergy to propofol or other drugs planned to be used in the trial; 7.Body mass index > 35 kg/m²; 8.There is a clear history of sleep disorders or severe circadian rhythm disruption; 9.Severe anemia, coagulation disorder, or severe liver and kidney dysfunction; 10.It is expected that drugs that may interfere with electroencephalography or the recovery of consciousness will need to be used during the operation, or the patient refuses to accept the intensive TMS-EEG monitoring and multiple venous blood collection specified in the protocol.

Design outcomes

Primary

MeasureTime frame
recovery neurodynamic slope;

Secondary

MeasureTime frame
Riker Sedation-Agitation Scor;3-minute delirium diagnostic scale;recovery quality scale;Post-Anesthesia Care Unit(PACU) stay time;full wake time;Numerical Pain Rating;Dynamic slope of weighted phase lag index between prefrontal-parietal brain regions in the theta frequency band (4-8 Hz) during recovery period;Montreal Cognitive Assessment;Open your eyes as instructed;Resting period Lempel-Ziv complexity values measured every minute during the recovery period;

Countries

China

Contacts

Public ContactZan Wang

Xuzhou Central Hospital

840547858@qq.com+86 177 1298 6638

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026