post-operative pain
Conditions
Interventions
Control Group C:Sufentanil 150ug+ Ondansetron 16mg
Experiment Group A:Taigiliding 5mg+ Ondansetron 16mg
Experiment Group B:Taigiliding 5mg+ Ondansetron 8mg
Sponsors
The First Hospital of Shanxi Medical University
Eligibility
Sex/Gender
Female
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: 1. Age: 18-65 2. The anesthesia method is general anesthesia, and the anesthesia grade is grade I to III. 3. The surgical method is gynecological laparoscopic surgery. 4. Those who, after the initial evaluation, can cooperate to complete the questionnaire survey and experiments; 5. Agree to participate in this study and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Refuse to participate in this study; 2. ASA Grade III or above; 3. History of chronic analgesic or sedative drug use includes benzodiazepines, alcohol abuse, and a history of allergy to anesthetic drugs; 4. If there are changes in the condition during the operation and rescue is required; 5. Preoperative severe cognitive dysfunction MMSE score =180mmHg;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative pain score;The demand for postoperative analgesia; | — |
Secondary
| Measure | Time frame |
|---|---|
| Postoperative delirium assessment;Sleep quality score;Assessment of delirium during the recovery period;QoR-15;The incidence of adverse events during anesthesia recovery; | — |
Countries
China
Contacts
Public ContactZhang Haibin
The First Hospital of Shanxi Medical University
Outcome results
None listed