Sinusitis
Conditions
Interventions
MGRNOX monitoring group (group A):MGRNOX monitor
Routine monitoring group (group B):Routine monitor
Sponsors
Department of Anesthesiology, Shenzhen Second People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1) aged 18-75 years; 2) patients undergoing elective sinus surgery under general anesthesia with endotracheal intubation; 3) Ethical: patients were willing to participate in the study and signed informed consent.
Exclusion criteria
Exclusion criteria: 1) ASA class IV or higher (e.g., Child-Pugh class C or preoperative dialysis) 2) patients with mental or neurological diseases or suspected dementia or memory impairment; 3) severe impairment of hearing, vision and language system; 4) confirmed/suspected abuse or long-term use of narcotic sedative and analgesic drugs; 5) Patients with contraindications or allergies to the trial drugs and other anesthetic drugs.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Recovery time of patients; | — |
Secondary
| Measure | Time frame |
|---|---|
| Intraoperative consumption of propofol;Intraoperative consumption of remifentanil; | — |
Countries
China
Contacts
Public ContactZhiheng Liu
Shenzhen Second People's Hospital
Outcome results
None listed