Benign uterine tumor
Conditions
Interventions
Group N:Saline
Sponsors
Department of Anesthesiology, Gansu Provincial Maternity and Child-care Hospital
Eligibility
Sex/Gender
Female
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Women >= 18 years old; 2. ASAI-II level; 3. Selective laparoscopic hysterectomy; 4. Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Refusing to participate in the research 2. BMI> 35kg/m2 3. History of chronic pain or taking any sedative and analgesic drugs 4. hypertension, arrhythmia and psychosis 5. Severe hepatic and renal insufficiency 6. Allergic to the ingredients of the study drug. 7. Has participated in other clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| QoR15;PSQI;Duration of surgery;Duration of anesthesia;Duration of pneumoperitoneum;Extubation time;PACU stay time;Hospital stay duration;Propofo consumption;Remifentanil consumption; | — |
Secondary
| Measure | Time frame |
|---|---|
| Incidence and severity of nausea and vomiting 24 hours after operation;Postoperative pain score;Demand of analgesic drugs ; | — |
Countries
China
Contacts
Public ContactXueyan Tao
Department of Anesthesiology, Gansu Provincial Maternity and Child-care Hospital
Outcome results
None listed