Depression
Conditions
Interventions
Concrol group:None
Experimental group:Preoperative administration of 0.2mg/kg esketamine by pump for 40 minutes
Sponsors
Xuanwu Hospital Capital Medical University
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1.18 7 points; 7. Have a clear understanding and voluntarily participate in the study, and sign the informed consent form by themselves.
Exclusion criteria
Exclusion criteria: 1. In addition to general venous anesthesia, other anesthesia methods are required, such as epidural and subarachnoid anesthesia; 2. Other types of surgeries other than those specified in the enrollment criteria; 3. Patients with severe abnormal liver and kidney function; 4. Refusal to use analgesic pump patients; 5. Presence of contraindications or caution to the use of esketamine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Recovery quality score on the first postoperative day; | — |
Secondary
| Measure | Time frame |
|---|---|
| The quality of recovery scores of the two groups on the third day after surgery and before discharge were performed;Comparison of depression tendency index between the two groups on the first and third days after surgery and before discharge;Comparison of analgesia between the two groups after surgery;Comparison of postoperative gastrointestinal function recovery between two groups;Adverse reaction incidence rate;Incidence of postoperative complications in two groups; | — |
Countries
China
Contacts
Public ContactWang Tianlong
Xuanwu Hospital Capital Medical University
Outcome results
None listed