Postoperative sleep disturbance
Conditions
Interventions
treatment group:Epidural esketamine+ropivacaine
Sponsors
Fudan University, Shanghai Cancer Center
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 18-75 years old , ASA I-III, Endoscopic or Da Vinci lower abdominal surgery,BMI<35
Exclusion criteria
Exclusion criteria: 1) No ability to sign informed consent, unable to communicate 2) Poorly controlled hypertension (preoperative blood pressure > 160/100) 3) Coagulation dysfunction 4) Allergic to ropivacaine 5) Intraocular hypertension and glaucoma 6) Known or suspected schizophrenia 7) Long-term poor sleep and a long history of taking sleeping pills 8) Severe coronary heart disease, a history of heart attack within 6 months, or chest pain after recent mild activity 9) Diagnosed sleep apnea syndrome
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sleep Quality; | — |
Secondary
| Measure | Time frame |
|---|---|
| depression and anxiety scores;Pain score;Adverse reactions;Consumption of opioid analgesics (sufentanil); | — |
Countries
China
Contacts
Public ContactJun Zhang
Fudan university, Shanghai Cancer Center
Outcome results
None listed