The research for EEG monitoring of nociceptive stimulation under general anesthesia

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200060419

Enrollment

Unknown

Registered

2022-06-01

Start date

2021-09-01

Completion date

Unknown

Last updated

2024-05-13

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

Conditions

None listed

Interventions

Case series:None

Eligibility

Sex/Gender

All

Age

18 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1. Signed and dated informed consent; 2. Promise to abide by the research procedures and cooperate with the implementation of the whole process of research; 3. Aged >=18 years and < 60 years; 4. ASA grade 1-2; 5. Patients who are expected to undergo elective surgery under general anesthesia.

Exclusion criteria

Exclusion criteria: 1. Patients with mental illness or taking antipsychotic drugs; 2. Diseases or injuries of the central nervous system; 3. Alcohol or drug abuse; 4. BMI > 28; 5. Patients with chronic pain or taking analgesics; 6. Severe impairment of auditory, visual and language systems; 7. Patients scheduled to be admitted to ICU after surgery; 8. Those who have infection, allergy, etc. at the site of the electroencephalogram monitoring electrode (forehead) are not suitable for attaching electrode; 9. Patients who participated in other clinical studies during the same period.

Design outcomes

Primary

Measure	Time frame
a wave;ß wave;sleep spindle;blood pressure;heart rhythm;d wave;EMG;	—

Countries

China

Contacts

Public ContactChen Xiangdong

Union Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology

xiangdongchen2013@163.com+86 15071096621

Outcome results