None
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: a. Age: 18-70 years old b, Type of surgery: laparoscopic total hysterectomy c, ASA classification: Grade I-III d, able to use pain scale, QoR-15 scale, sleep quality scale and operate intravenous PCA device e, Understanding and willingness to participate in the trial, signed informed consent by themselves or their immediate family members
Exclusion criteria
Exclusion criteria: a. Clear preoperative allergy or hypersensitivity to test drugs (acetaminophen and mannitol); b. Impairment of vital organs such as impaired liver function (transaminases = twice the upper limit), patients with active liver disease, chronic hepatitis, cirrhosis of the liver, chronic kidney disease, renal insufficiency (creatinine = 2.0 mg/dl), chronic malnutrition, and known or suspected history of alcohol or drug abuse; c. Pregnant or lactating patients; d. Those who require preoperative sleep aids with tranquilizers; e. severe hypovolemia (due to dehydration or blood loss), glucose-6-phosphatase dehydrogenase deficiency; f. The presence of trauma, infection or dermatitis at the puncture site that precludes nerve block operation; g. patients with preoperative cognitive dysfunction.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain visual analog score;QoR-15;Sleep quality score; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative opioid consumption;rescue analgesia rate;Incidence of anesthesia-related adverse reactions;Antiemetic rescue rate; | — |
Countries
China
Contacts
Zhongshan Hospital of Fudan University, Xiamen Branch