Clinical study of postoperative analgesia in cesarean section
Conditions
Interventions
Group1:Add 20mg nalbuphine to local anesthetic for transverse abdominal plane block (bilateral)
Group2:Add 30mg nalbuphine to local anesthetic for transverse abdominal plane block (bilateral)
Group3:Simple transverse abdominis plane block
Sponsors
Liaocheng People's Hospita
Eligibility
Sex/Gender
Female
Age
20 Years to 35 Years
Inclusion criteria
Inclusion criteria: 1. Patients undergoing cesarean section; 2. American Society of Anesthesiologists (ASA) grade II~III; 3. Aged 20 ~ 35 years old, weight 50-90kg.
Exclusion criteria
Exclusion criteria: 1. Those allergic to nalbuphine and ropivacaine; 2. Damaged skin infection at the puncture site; 3. Mental abnormalities; 4. Have obvious heart, lung, liver and kidney insufficiency; 5. Cannot use the numerical rating scale (NRS) score of pain; 6. Those who refuse to perform nerve block.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Postoperative resting and activity NRS scores;Pain location: visceral pain or body surface pain;Postoperative analgesics (including PCIA dosage and additional analgesics in the ward); | — |
Secondary
| Measure | Time frame |
|---|---|
| Nerve block plane;Intestinal motility recovery time, eating time, getting out of bed activity time;Patient comfort, postoperative adverse reactions, satisfaction with postoperative analgesia and postoperative recovery; | — |
Countries
China
Contacts
Public ContactAi'lan Yu
Outcome results
None listed