Postoperation pain
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: a) Age 40-65 years old b) BMI18 ~ 30kg/m2 c) ASA Grade I ~ III. d) Patients undergoing laparoscopic total abdominal hysterectomy e) Voluntarily sign informed consent
Exclusion criteria
Exclusion criteria: a) Patients with contraindications to regional block; b) People who are allergic to the drugs used in the study or who have absolute contraindications in their use; c) Severe cardiovascular and cerebrovascular, liver and kidney insufficiency or arrhythmia; d) Have a history of mental illness or long-term history of taking psychotropic drugs or chronic analgesic drugs; e) Severe visual and writing defects or speech communication disorders; f) Patients with malignant tumors; g) The patient refuses to participate or the investigator considers the patient unfit to participate in the clinical trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Analgesic effect in 0-72h after operation; | — |
Secondary
| Measure | Time frame |
|---|---|
| Remedial analgesia ; | — |
Countries
China
Contacts
Linyi People's Hospital