None
Conditions
Interventions
Control group:None
Experimental group:Anesthesia psychological visit
Sponsors
Nanchong Central Hospital of Sichuan Province
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: Patients with elective surgery, no history of drug allergy, no sleep disorders, and no history of mental illness volunteered to participate in this study and signed a written informed consent for anesthesia.
Exclusion criteria
Exclusion criteria: A history of addiction to sedatives, opioids, and alcohol before surgery; Allergy to narcotic drugs; Ischemic cerebrovascular disease; Patients with liver and kidney dysfunction, cardiovascular diseases and endocrine diseases; Smoking within 2 weeks; Have a severe neurological disorder or cognitive impairment; Language dysfunction; Change the surgical plan.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Quality of postoperative recovery Table -15(QOR-15); | — |
Secondary
| Measure | Time frame |
|---|---|
| Generalized anxiety Scale-7(GAD-7);GeneralSelf-Efficacy Scale(GSES);Visual analogue scale(VAS); | — |
Countries
China
Contacts
Public ContactWuchang Fu
Nanchong Central Hospital
Outcome results
None listed