Postoperative pain
Conditions
Interventions
TK group:Postoperative ketorolac mixed bupivacaine with TAP block,Postoperative intravenous controlled analgesia
T group:Postoperative simple bupivacaine with TAP block,Postoperative intravenous ketorolac,Postoperative intravenous controlled analgesia
C group:Postoperative intravenous ketorolac,Postoperative intravenous controlled analgesia
Sponsors
Obstetrics and Gynecology Hospital of Fudan University
Eligibility
Sex/Gender
Female
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Aged 18-60 years; ASA Grade I-II; Elective laparoscopic gynecologic surgery and asked for postoperative intravenous analgesia; patients who can fully communicate and use PCA devices correctly; informed consent of the subjects and signed consent.
Exclusion criteria
Exclusion criteria: Patients with a history of narcotic analgesics, sedatives or non-steroidal anti-inflammatory drugs; Patients with a history of allergies to the use of this study; Patients with a history of neuromuscular disease, history of cardiovascular disease, history of endocrine system disease, history of allergic disease, history of mental illness; BMI > 30kg/m2 or BMI < 18kg/m2; Patients with a history of peptic ulcer and/or bleeding; Coagulation dysfunction; Pregnancy or lactation women; Addict to drugs or alcohol; Researchers believed that patients who are not suitable for clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Number of postoperative analgesic pump compressions;Postoperative analgesia pump drug consumption; | — |
Secondary
| Measure | Time frame |
|---|---|
| age;height;weight;BMI;duration of surgery;Blood pressure;heart rate;oxygen saturation;rest pain;activities of pain;NVAS;Exhaust time;The number of days in hospital; | — |
Countries
China
Contacts
Public ContactQi Jiang
Obstetrics and Gynecology Hospital of Fudan University
Outcome results
None listed