Postoperative sleep
Conditions
Interventions
Test group:Ultrasound-guided stellate ganglion block before anesthesia induction
Control group:None
Sponsors
Shenzhen Longgang Central Hospital
Eligibility
Sex/Gender
Female
Age
40 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. American Society of Anesthesiologists (ASA) physical status classification I-II; 2. Patient age between 40-60 years old; 3. Planned laparoscopic surgery (total laparoscopic hysterectomy or myomectomy); 4. Willing to accept postoperative patient-controlled intravenous analgesia pump.
Exclusion criteria
Exclusion criteria: 1. The patient refuses to participate in the study; 2. Body mass index (calculated by dividing weight in kilograms by height in meters squared) is above 30; 3. Preoperative Pittsburgh Sleep Quality Index (PSQI) is above 7; 4. Patients allergic to local anesthetics; 5. Coagulation disorders and abnormal anatomy of the neck or shoulder; 6. Those who have previously relied on sleeping pills to fall asleep; 7. Cognitive impairment or unable to communicate; 8. Unable to use the patient-controlled intravenous analgesia pump.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative sleep quality; | — |
Secondary
| Measure | Time frame |
|---|---|
| Hospital Anxiety and Depression Scale score;Postoperative pain score; | — |
Countries
China
Contacts
Public ContactZhang Yanli
Shenzhen Longgang Central Hospital
Outcome results
None listed