Postoperative analgesia
Conditions
Interventions
None listed
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Female, age >= 18 years and < 60 years, ASA I-III; 2. Plan to perform gynecological laparoscopic surgery under general anesthesia and require postoperative PCIA analgesia; 3. Having normal communication ability, could use the postoperative patient-controlled intravenous analgesia pump correctly, and could cooperate to evaluate the pain intensity; 4. No history of narcotic drug allergy; 5. Be able to understand the informed consent contents and make judgments independently, agree to participate in this study and able to sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Mental illness and cognitive defects; 2. Allergic to known analgesic and sedative drugs; 3. With a history of chronic pain or have a long history of using analgesic and sedative drugs; 4. Patients with peripheral neuropathy symptoms or liver and kidney function abnormality; 5. Failure to implement as designed protocol, incomplete data records, or affecting the judgment of pain intensity; 6. Patient refused.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Visual analog scale, VAS; | — |
Secondary
| Measure | Time frame |
|---|---|
| Total amount of analgesic drugs;Patient self-rated satisfaction;Pain Catastrophizing Scale, PCS;Pain Sensitivity Questionnaire, PSQ; | — |
Countries
China
Contacts
Chongqing Health Center for Women and Children