Postoperative nausea, vomiting and postoperative sleep disturbance
Conditions
Interventions
Experimental group:0.2% ropivacaine 5ml
Control group:Saline 5ml
Sponsors
The Second People's Hospital of Kashgar Prefecture
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Having at least one high-risk factor for PONV includes no history of smoking, a history of PONV, a history of motion sickness, or the need for opioid analgesia after surgery. There was no abnormality of liver and kidney function before surgery; no coagulation disorder; no local skin infection; no recent history of myocardial infarction, abnormal cardiac excitation conduction; no glaucoma, goiter, hypertension, coronary heart disease; and the patient was cooperative without mental disorder.
Exclusion criteria
Exclusion criteria: Pregnant and postpartum women, lactating women, patients with psychoneurological diseases, pacemakers, gastroesophageal reflux disease, and patients with contraindications to ropivacaine and lidocaine.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pittsburgh Sleep Quality Index;PONV grading and antiemetic remedy status; | — |
Secondary
| Measure | Time frame |
|---|---|
| Surgical time and anesthesia time;Intraoperative sufentanil dosage, infusion volume, and bleeding volume;Extubation time, PACU stay time;VAS pain score during 24-hour postoperative activity (cough);Remedial status of analgesic drugs;Postoperative first time out of bed and postoperative hospitalization time;Incidence of SGB related complications such as local anesthetic poisoning, pneumothorax, recurrent laryngeal nerve block, etc; | — |
Countries
China
Contacts
Public ContactLiu Huan
The Second People's Hospital of Kashgar Prefecture
Outcome results
None listed